0440637 5 EN Fin Lock Surgical Technique

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Integra®

Titan™ Modular Shoulder System, 2.5

Featuring Fin-Lock™ Surgical Technique

SURGICAL TECHNIQUE

Table of Contents

Introduction

Indications ............................................................................................................................................................................................................ 2

Contraindications ................................................................................................................................................................................................ 2

Warnings ............................................................................................................................................................................................................... 2

Precautions ............................................................................................................................................................................................................ 3

Sterility ...................................................................................................................................................................................................................3

Adverse Events ......................................................................................................................................................................................................3

Surgical Technique – Visual Step By Step ....................................................................................................................................................... 4

Design Rationale ................................................................................................................................................................................................. 6

Surgical Technique

Step 1: Preoperative Templating and Patient Positioning ..............................................................................................................................7

Step 2: Exposure ................................................................................................................................................................................................... 7

Step 3: Subscapularis Tendon Management ....................................................................................................................................................8

Step 4: Capsule Release and Humeral Head Dislocation .............................................................................................................................. 9

Step 5: Humeral Head Preparation and Resection ........................................................................................................................................ 10

Step 6: Glenoid Preparation and Implantation

Step 6a: Fin-Lock™ Glenoid Preparation and Implantation ................................................................................................................ 13

Step 6b: Pegged Glenoid Preparation and Implantation .................................................................................................................... 17

Step 6c: Keeled Glenoid Preperation and Implantation ......................................................................................................................19

Step 7: Humeral Canal Preparation ................................................................................................................................................................. 20

Step 8: Body and Stem Trial Insertion ............................................................................................................................................................. 21

Step 9: Humeral Head Trial ...............................................................................................................................................................................21

Step 10: Soft Tissue Balancing and Trial Removal ........................................................................................................................................ 23

Step 11: Preparation for Repair of Subscapularis Tendon ............................................................................................................................ 23

Step 12: Body and Stem Implant Assembly ................................................................................................................................................... 23

Step 13: Stem/Body Implantation and Head Assembly ............................................................................................................................... 24

Step 14: Revision Procedure ............................................................................................................................................................................. 26

Long Stem Option ............................................................................................................................................................................................. 26

Step 15: Wound Closure. .................................................................................................................................................................................. 28

Postoperative Therapy Protocol ..................................................................................................................................................................... 29

Instrumentation ................................................................................................................................................................................................. 30

Ordering Information and Implant Dimensions ............................................................................................................................................ 41

Total Shoulder Arthroplasty or Hemiarthroplasty is indicated for:

• Severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis.

• Fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood

supply or where the surgeon’s experience indicates that alternative methods of treatment are unsatisfactory.

• Other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable

(e.g. revision of a failed primary component).

Shoulder Hemiarthroplasty is also indicated for:

• Ununited humeral head fractures

• Avascular necrosis of the humeral head

• Rotator cuff arthropathy

• Deformity and/or limited motion

The humeral component is intended for cemented or uncemented use. The glenoid component is intended

for cemented use only.

Contraindications

The following conditions are contraindications for total shoulder arthroplasty and hemiarthroplasty:

• Active local or systemic infection

• Inadequate bone stock in the proximal humerus or glenoid fossa for supporting the components

• Poor bone quality, such as osteoporosis, where there could be considerable migration of the prosthesis and/or

a chance of fracture of the humerus or glenoid

• Absent, irreparable or nonfunctional rotator cuff or other essential muscles

• Pregnancy

• Muscular, neurologic, or vascular deficiencies that compromise the affected extremity

• Known metal allergies

The following conditions are contraindications for total shoulder arthroplasty and hemiarthroplasty:

• Absent, irreparable or nonfunctional rotator cuff or other essential muscles

Warnings

The use of a glenoid prosthesis in patients with cuff tear arthropathy could increase the risk of glenoid component loosening

due to non-anatomic loading conditions. The following conditions tend to adversely affect shoulder replacement implants:

• Excessive patient weight

• High levels of patient activity

• Likelihood of falls

• Poor bone stock

• Metabolic disorders

• Disabilities of other joints

ESSENTIAL PRODUCT USE INFORMATION: For additional important information pertaining to the use of this product, please see product package insert.

This information was current at the time of printing, but may have been revised after that date.

Indications

Precautions

• Do not reuse this device. Reuse of this product may result in infection or other systemic complication that may affect the

patient’s overall health. Additionally, the reuse of this product could adversely affect function of the device. Any implant

that has been damaged, mishandled, or removed from the sterile field may have surface damage that could result in

implant fracture and/or particulate and should be discarded.

• The Titan™ Modular Shoulder System has not been evaluated for safety and compatibility in the MR environment. It has

not been tested for heating, migration, or image artifact in the MR environment. The safety of the Titan Modular Shoulder

System in the MR environment is unknown. Scanning a patient who has this device may result in patient injury.

Sterility

The Fin-Lock™ Glenoid implant has been sterilized by Ethylene Oxide (EO) and is sterile in the unopened, undamaged

package. If either the implant or the package appears to be damaged or has been opened, or if sterility is questioned for any

reason, the implant should not be used. Do not resterilize this product. All other Titan™ System Implants have been sterilized

by gamma radiation and are sterile in the unopened, undamaged package. If either the implant or the package appears

damaged or has been opened, or if sterility is questioned for any reason, the implant should not be used. Do not resterilize

this product.

Adverse Events

• Potential adverse events include early or late postoperative infection, allergic reaction, intraoperative or postoperative bone

fracture and/or postoperative pain.

• Intraoperative bone perforation or fracture may occur, particularly in the presence of poor bone stock caused by

osteoporosis, bone defects from previous surgery, bone resorption, or while inserting the device.

• Loosening or migration of the implants can occur due to loss of fixation, trauma, malalignment, bone resorption, and/or

excessive activity.

• Surgical intervention may be required to treat adverse effects.

• MDR Reporting Reminder: Medical device manufacturers and users are required by law and regulation to report serious

injuries and death.

Exposure

Surgical Technique – Visual Step By Step with Fin-Lock™ Glenoid

Head Resection

Size and place wire

Drill peripheral holes Punch

Trial

Ream Drill center holes

Implant

Final Glenoid

Implantation

Trialing Distal Stem

and Proximal Body

Osteotomy,

Evaluation &

Head Trialing

Head

Assembly

Final Humeral

Implantation

Implant

Assembly

Surgical Technique – Visual Step By Step with Fin-Lock™ Glenoid (continued)

Design Rationale

Redefining Modularity

• 26 Humeral Head options based on published anthropomorphic data of over 300 human humeri to provide

anatomic fit by respecting the varying radius of curvature which allows for simplified sizing and soft tissue

balancing.

1,2

• Interchangeable proximal bodies and distal stems to accommodate varying patient anatomy.

Platform Convertibility

• Well-fixed press-fit stem options provide an intraoperative building platform and a pathway for revision.

• Modularity allows for convertibility from Total Shoulder Arthroplasty to Reverse Shoulder Arthroplasty with

version adjustment.

Enhanced Instrumentation

• Compaction technique to impact and preserve bone.

• Consistent instrumentation is utilized for primary, fracture and revision procedures aiding in familiarity and more

efficient use of space.

1. Iannotti JP, Gabriel JP, Schneck SL, et al: The normal glenohumeral relationships. An anatomical study of one hundred and forty shoulders. J Bone Joint Surg (Am), 1992; 74:491-500.

2. Hertel R, Knothe U and Ballmer F: Geometry of the proximal humerus and implications for prosthetic design. J Shoulder Elbow Surg. Vol. 11, No 4, 2002; 331-338.

Body

Screw

Fin-Lock™ Glenoid

• Center peg features fins to

aid in stability

• Highly crosslinked polyethylene

for improved wear resistance

Pegged Glenoid

Eccentric

Head

Keeled Glenoid

Fin-Lock™ Glenoid

Press-Fit

Stem

Cemented

Stem

Concentric

Head

Fracture

Body

Screw

Primary

Body

1 - 1

2 - 1

2 - 2

Step 1 • Preoperative Templating

and Patient Positioning

Preoperative evaluation of the humerus using the Titan

Modular Shoulder System X-ray Templates helps determine the

size of the prosthesis and level of the humeral head resection.

The goal is to remove the humeral head at the anatomic neck

using the patient’s own neck shaft angle, generally between

130-135°, and humeral version indicated by the patient’s natural

version.

1 - 1

Hemi and Total Shoulder Arthroplasty can be performed using

general anesthesia, regional anesthesia (i.e., interscalene block),

or a combination. Place the patient in beach chair position.

This position would have the patient supine with the hips

flexed approximately 30°, knees bent approximately 30° and

back elevated approximately 30°. Specialized headrests, such as

the MAYFIELD® or the McConnell, arm mounts or operating

tables with breakaway side panels can facilitate further access

to the top and back of shoulder.

Step 2 • Exposure

A deltopectoral approach is used to provide exposure to the

anterior aspect of the glenohumeral joint, the upper humeral

shaft and the humeral head. The initial incision line runs from

the mid-clavicle, over the top of the coracoid and extends in a

straight line down the anterior aspect of the arm. It should

follow the path of the cephalic vein along the interval between

the deltoid and the pectoralis major. The length of the

initial incision along this line can vary, depending on the

exposure needed to provide adequate access and visualization

of the joint, and is determined by patient body habitus.

Once the initial incision is made, expose, incise and release the

fascia. Locate the cephalic vein at the deltopectoral interval.

Separate the deltoid and pectoralis major muscles so that

the deltoid muscle is completely free from its origin to its

insertion, especially along its deep surface. Abduct and

externally rotate the arm. Gently retract the cephalic vein

medially or laterally along with the deltoid and pectoralis

muscle.

2 - 1

As the manufacturer of this device, Integra does not practice medicine and does not recommend this or any

other surgical technique for use on a specific patient. The surgeon who performs any implant procedure is

responsible for determining and using the appropriate techniques for implanting the device in each patient.

Caution: Federal law restricts this device to sale by or on the order of a physician or practitioner.

Surgical Technique

The Titan Modular Shoulder System was developed in conjunction with Joseph Abboud, MD; Phillip Duke, MB.BS, FRACS, FA(ORTH)A;

William Geissler, MD; Sanford Kunkel, MD; Anand Murthi, MD; Matthew Ramsey, MD; Mark Ross, MB.BS, FRACS, FA(ORTH)A

3 - 1

3 - 2

However, a small triangle can be removed from the coracoacromial ligament which will allow visualization of the

subscapularis and supraspinatus interval.

Release the biceps tendon from the bicipital groove and along the rotator interval down to its glenoid attachment.

Resect the long head of the biceps at the origin of the superior glenoid. Open the rotator interval along the line of the

biceps to define the superior margin of the subscapularis.

Isolate, clamp and ligate or coagulate the anterior humeral circumflex vessels lying across the anterior/inferior third of

the subscapularis tendon.

It is important to be aware of the musculocutaneous nerve, which penetrates the coracobrachialis muscle

2.54cm-5.08cm distally from the coracoid. The nerve may not be palpable within the surgical field, but remember its

proximity to the conjoined tendon. Digitally locate the axillary nerve. Introduce a Hohmann retractor and carefully

retract the nerve along with the latissimus dorsi tendon. This is especially important as it will protect the axillary nerve,

define and expose the inferior capsule.

Step 3 • Subscapularis Tendon Management

Lesser Tuberosity Osteotomy

Locate the insertion of the subscapularis tendon onto the lesser

tuberosity. Place the saw blade or osteotome just lateral to the

subscapularis insertion point and osteotomize approximately 4-5mm

of the lesser tuberosity.

3 - 1

3 - 2

Subscapularis Tenotomy

Alternatively the tendon can be removed from its insertion with

sharp dissection about 1cm medial to the lesser tuberosity. This

will allow for tendon to tendon reattachment of the subscapularis.

Step 2 • Exposure (continued)

Incise the clavipectoral fascia lateral to the conjoined tendon. If needed, release the upper 25% of the pectoralis major

tendon from its insertion on the humerus, using an electrocautery cutting blade. Place a Hohmann retractor over the

top of the humeral head, pulling the upper part of the deltoid posteriorly.

Check that rotator cuff tendons are intact. Introduce self-retaining Weitlander and Kobel retractors underneath

conjoined tendon and underneath the middle deltoid. It is important to always save or preserve the coracoacromial

ligament.

2- 2

Note

If the capsule is tented over large inferior osteophytes, it may be safer to remove the osteophytes with an

osteotome, moving away from the articular surface in an inferior direction. Once the osteophyte has been separated

from the bone, it may be peeled off the capsule, and the capsular release can then be completed adjacent to the

capsular attachment to the humerus. This decreases the risk of inadvertently damaging the axillary nerve when

attempting to mobilize the capsule out from beneath large inferior osteophytes.

Place a large Darrach retractor underneath the upper part of

the humeral head and dislocate the humerus. Put a medium

size retractor on the inferior part of the humeral head and

continue to bring the arm into full external rotation. The

entire humeral head should now be in vision, with all

capsular tissues removed from around the neck to provide

excellent exposure.Release of the anterior, inferior and

posterior glenohumeral ligaments is vital to properly and

concentrically centralize the humeral head as noted above.

At this point, the humeral head should freely rotate into

maximum external rotation, slight abduction and significant

extension allowing the head to dislocate anteriorly for

preparation of the humeral head. Proper anterior and inferior

capsular releases are needed for ease of dislocation and

proper humeral head preparation as well as re-establishing

concentricity of the glenohumeral joint. Releasing the

inferior capsule off the humerus past the 6 o’clock position

is essential in gaining exposure. Bone preparation is initiated

by debridement of sufficient amount of anterior inferior

osteophytes to properly identify the anatomic neck.

4 - 3 4 - 3

4 - 1

4 - 2

Step 4 • Capsule Release and Humeral Head Dislocation

Using blunt dissection, separate the capsule from the subscapularis,

inferiorly and medially. Release the rest of the anterior capsule from

the subscapularis to the glenoid rim. Release the coracohumeral

ligament from the base of the coracoid. Place traction sutures in the

subscapularis tendon to control and mobilize it from the anterior

glenoid neck. The subscapularis traction sutures will be utilized as a

“shoe horn” to control the humeral head dislocation and relocation.

The ‘subscapularis tendon-capsule complex’ is dissected and elevated

as one unit from the humerus at the medial aspect of the bicipital

groove. If this complex is contracted, a superior 180° release of the

subscapularis must be performed to mobilize the tendon to gain

eventual external rotation.

4- 1

4 - 2

Further humeral neck joint capsule release may be performed medially,

anteriorly or inferiorly as needed. The posterior capsule is maintained to

facilitate centralization and prevent posterior subluxation. Take care to protect the axillary nerve as it passes inferior to

the subscapularis and capsule. The location of the axillary nerve should be kept in mind at all times during capsular

release.

30°

Head Resection with an Intramedullary Cutting Guide

Attach the T-Handle to the Starter Awl and create a pilot hole at the top of the humerus,

in line with the long axis of the humerus just lateral to the articular surface of the head

of the humerus and medial to the attachment of the rotator cuff.

5 - 2

The Head Cutting Depth Gauge can be used to assess the

cutting plane. The gauge should enter the anterior surface of

the humerus along the line of the anatomic neck and exit

2-3mm proximal to the posterior cuff attachment. Before the

oscillating saw blade (33 x 0.8mm) is placed along the flat

surface of the cutting plate, drill two 3.2mm Fixation Pins

through the cutting plate and into the underlying bone which

will stabilize the guide. Remove the Cutting Guide-Starter Awl

assembly by loosening knob 3 on the cutting plate and

removing the Starter Awl out of the humerus. Use an

oscillating saw through the capture to remove the humeral

head. If additional head resection is needed, lower the blade to

the next slot. This will remove 3mm of additional bone. After

removing the humeral head, extract the Fixation Pins using the

Pin Puller.

5 - 3

5 - 2

5 - 3

30°

5 - 4

Note

This surgical step should not be performed with power reamers or drills.

Leave the Starter Awl in place and clamp the Head Cutting Guide around the awl by

tightening knob 1. The Version Rod is then passed through the holes in the cutting guide

and is rotated into the desired retroversion. The holes denote 20°, 30°, and 40° of

retroversion, in reference to the forearm axis. If more or less retroversion is required,

use the orientation holes on the cutting guide collar and rotate the forearm to desired

angle accordingly. Slide the cutting plate against the humerus and tighten knob 2.

Then adjust the resection level by sliding the cutting plate up or down and tightening

knob 3.

Step 5 • Humeral Head Preparation and Resection

Assess the humeral head and remove any unwanted osteophytes to return the proximal humerus to near native anatomy.

Freehand Head Resection Technique

Place the Head Cutting Template along the anterior aspect of the arm

parallel to the shaft of the humerus, and mark the angle at which the

humeral head will be resected with an oscillating power saw or mallet and

large osteotome. There are two proximal holes on the Head Cutting

Template for 3.2mm Fixation Pin placement, if preferred. A 30° threaded

version hole for the Head Cutting Template Handle / Version Rod is also

available to assess retroversion.

The saw or osteotome should enter the anterior surface of the humerus

along the line of the anatomic neck and exit 2-3mm proximal to the

posterior cuff attachment. Once complete, the resection should be at the

level of the articular surface of the supraspinatus insertion site.

30°

5 - 1

Note

For larger canals, it may be preferable to start impacting up, using the Stem Trials, until a solid fit is achieved in the

canal. The cutting guide can then be attached to the Stem Trial Handle in the same manner as above.

Head Sizing

Use the Head Sizing Gauge to measure the resected head diameter

and thickness. Be sure to remove all osteophytes for accurate sizing.

After measuring and selecting the humeral head size, place the

humeral head on the back table to remove the cancellous bone. Use

the cancellous graft later in the procedure if impaction bone grafting

is needed for the metaphyseal body and humeral distal stem.

5 - 5 5 - 5

Note

The Humeral Osteotomy Covers provided in the instrument

tray can be used to protect the proximal humeral

preparation area.

Step 5 • Humeral Head Preparation and Resection (continued)

Step 6 • Glenoid System Preparation and Implantation

Exposure

Place a Fukuda retractor in the joint to retract the humerus posteriorly. Identify the axillary nerve by digital palpation and place a

blunt Hohmann retractor between the axillary nerve and the subscapularis. Dissect the inferior capsule from the inferior border

of the subscapularis. Release the capsule above the blunt Hohmann retractor to the glenoid margin. Release the rotator interval

to the base of the corocoid to complete the superior and inferior release of the subscapularis. Release the capsule between the

labrum and the subscapularis, leaving the labrum attached to the glenoid. With the subscapularis circumferentially released,

the remnant capsule on the undersurface of the subscapularis can either be resected or retained to bolster the bulk of the

subscapularis. Place the subscapularis with its attached tuberosity fragment behind a retractor. Grasp the remaining biceps tendon

and excise the posterosuperior labrum from within the joint to the inferior labrum. Similarly, excise the anterosuperior labrum to

the inferior labrum. This leaves a small fragment of inferior labrum with attached capsule that needs to be released. Protect the

axillary nerve with an index finger and release the inferior capsule from the labrum. After release of the inferior capsule, exposure

to glenoid is improved. Glenoid exposure is complete once the inferior capsule is released and the remnant labrum is excised.

6a: Fin-Lock Glenoid 6b: Pegged Glenoid 6c: Keeled Glenoid

Pegged Glenoid Keeled Glenoid

Fin-Lock Glenoid

Insert the 2.8mm Guide Wire through the selected Sizer. Advance the Guide Wire until adequate purchase is achieved in the

glenoid. Remove the Angled Handle and slide the Sizer anteriorly to remove, leaving the guide wire in the bone. The Glenoid

Holder can be used to remove the sizer. Do not grasp the Sizer at the hex to prevent damaging the connection with the handle.

Note

Optional version-correction Sizers are included in the tray. Assess

posterior wear on the glenoid and if version correction is necessary,

select the appropriate 5 or 10 degree Sizer to accommodate off

centered reaming and retroversion correction. The amount of

version correction is typically established on preoperative CT scan.

If more than 10° to 15° of version correction is required, asymmetric

reaming of the glenoid will not adequately correct the version

without compromising glenoid implantation.

6a- 1

Size Selection and Guide-Wire Placement

Select a Fin-Lock Sizer and attach the Angled Handle to the center post of

the Sizer. The handle can be adjusted to an anterior superior angle. Select

the size that covers as much of the glenoid surface as possible, without

overhanging the periphery of the bone.

6a- 1

Version Correction Step Height

None +0 mm

5º +3 mm

10º +5 mm

6a: Fin-Lock Glenoid System

Cannulated Glenoid Preparation

Head Size

(mm)

Spherical

Radial

Mismatch with

ExtraSmall

Glenoid (54 Ø)

Radial Mismatch

with Small

Glenoid (59 Ø)

Radial

Mismatch

with Medium

Glenoid (64 Ø)

Radial

Mismatch

with Large

Glenoid (66 Ø)

38x14* 41 6.5mm 9.0mm 11.5mm 12.5mm

40x15* 43 5.5mm 8.0mm 10.5mm 11.5mm

42x16 45 4.5mm 7.0mm 9.5mm 10.5mm

44x16 48 3.0mm 5.5mm 8.0mm 9.0mm

44x19 45 4.5mm 7.0mm 9.5mm 10.5mm

46x14 54 0.0mm 2.5mm 5.0mm 6.0mm

46x17 49 2.5mm 5.0mm 7.5mm 8.5mm

46x20 47 3.5mm 6.0mm 8.5mm 9.5mm

48x15 56 -1.0mm 1.5mm 4.0mm 5.0mm

48x18 51 1.5mm 4.0mm 6.5mm 7.5mm

48x21 49 2.5mm 5.0mm 7.5mm 8.5mm

50x19 53 0.5mm 3.0mm 5.5mm 6.5mm

50x22 51 1.5mm 4.0mm 6.5mm 7.5mm

52x20 55 -0.5mm 2.0mm 4.5mm 5.5mm

*38mm and 40mm Offset/Eccentric Head option only.

*Green boxes represent the ideal glenohumeral sizing options as it relates to the Humeral Head and

Glenoid implant sizes.

48 mm x 15mm Head:

Spherical Diameter = 56mm

Medium Glenoid:

Spherical Diameter = 64mm

Diametrical Mismatch = 8mm

Radial Mismatch = 4mm

Note

When sizing the glenoid, care should be taken to create the recommended 4.0 - 8.5mm radial mismatch

of the Humeral Head and Glenoid components. See chart below.

Step 6 • Glenoid System Preparation and Implantation (continued)

6a-2

Cannulated Glenoid Reaming

Select the appropriate sized Cannulated Reamer and attach the

reamer to the 2.8mm Drill Shaft. Start the reamer prior to

contacting the glenoid surface. Ream accordingly until proper

concavity has been achieved and cartilage has been removed.

Remove the reamer, leaving the Guide Wire in the bone. It is

important to remember that over-reaming will both decrease

the surface area of the glenoid face and reduce the depth of

the glenoid vault. Excessive glenoid reaming should be avoided

(See recommendations, in section 6a-1, on the limits of asymmetric

glenoid reaming)

If manual reaming is preferred, attach the 2.8mm Drill Shaft to

the T-Handle located in the Fin-Lock instrument tray.

6a-3

Cannulated Center Peg Preparation

Select the appropriate Cannulated Central Peg Drill: 15mm

for XS/S and 18mm for M/L. Attach the Cannulated

Central Peg Drill to the 2.8mm Drill Shaft. Slide the drill

over the Guide Wire and drill to the stop. Remove the

Guide Wire. Attach the Angled Handle to the Drill Guide

and align the Drill Guide over the central hole. Place a

Central Anti-Rotation Peg to stabilize the Drill Guide.

Continue to step 6a-7

6a-3

6a-4

Size selection

Select a Fin-Lock Sizer and attach the Angled Handle to the

center post of the Sizer. The handle can be adjusted to an

anterior superior angle. Select the size that covers as

much of the glenoid surface as possible, without

overhanging the periphery of the bone.

6a-2

6a-4

Non-Cannulated Glenoid Preparation

6a: Fin-Lock Glenoid System (continued)

6a-5

Glenoid Reaming

Attach the Starter Drill to the 2.8mm Drill Shaft. Select

the appropriate Starter Drill Guide and align the guide

centrally on the glenoid. Drill through the center hole

until the drill stops to create a hole for the

non-cannulated reamer post.

Select the appropriate Non-Cannulated reamer and attach

it to the 2.8 mm Drill Shaft. Start the Reamer prior to

contacting the glenoid surface. Ream accordingly until

proper concavity has been achieved and cartilage has been

removed. It is important to remember that over-reaming

will both decrease the surface area of the glenoid face and

reduce the depth of the glenoid vault. Excessive glenoid

reaming should be avoided.

If manual reaming is preferred, attach the 2.8mm Drill Shaft

to the T-Handle located in the Fin-Lock instrument tray.

6a-6

Center Peg Preparation

Attach the Angled Handle to the 2.8mm Drill Guide.

Select the appropriate Central Peg Drill: 15mm for XS/S

and 18mm for M/L. Attach the Central Peg Drill to the

2.8mm Drill Shaft. Align the Drill Guide with the center

hole and drill until the collar of the drill bit contacts the

guide. Place a Central Anti-rotation Peg in the hole.

Option: An alternative to holding the Drill Guide in place

is to insert the 2.8mm Guide Pin through one of two

holes in the Drill Guide directly and securely into the

glenoid fossa. This alleviates the need to hold the Drill

Guide in place by hand, and allows for better visibility

and maneuverability in the joint space.

6a-7

Peripheral Peg preparation

Attach a Peripheral Drill to the Self-retaining

Drill Adaptor. Ensure the Drill Guide is

aligned so that the two adjacent holes are

inferior. Drill the superior hole (1) until the

collar of the drill bit contacts the guide. Pull

the Self-retaining Drill Adaptor gently and

the drill will remain in the hole and act as an

anti-rotation peg. Select another Peripheral

Drill and drill the posterior inferior (2), hole.

Leave the drill in as an anti-rotation peg.

Select another Peripheral Drill and drill the

anterior inferior hole (3). Remove the Drill

Guide, Central Anti-rotation Peg and

Peripheral Drills.

Note

Peripheral drills should be left in

place to act as an anti-rotation peg.

6a-5

6a-6

6a-7

6a: Fin-Lock Glenoid System (continued)

6a-8

Punch

A Punch is available to check hole positioning/depth in

addition to being used as a cement pressurizer. Check

each peripheral hole to determine whether it penetrates

the scapula at its base. If penetration is detected consider

bone grafting the hole with cancelleous bone harvested

from the resected humeral head. The Punch can be

utilized to impact the graft.

6a-9

Trial

Select the appropriate Fin-Lock Trial and impact the trial

onto the glenoid using the Glenoid Impactor. The trial

matches the drill diameter and will give you a secure trial fit.

Visually verify that the trial component sits flush with the

prepared glenoid surface through the slots in the trial.

Remove the trial and irrigate the glenoid using pulsative

lavage to remove blood and tissue debris from the drill holes.

6a-10

Cement and Implant

While cement is being prepared, obtain hemostasis by

packing each of the peg holes with thrombin and surgical

gauze or gel foam. Mix cement using manual or syringe

application. Place the cement into a 60 cc Catheter/Toomey

syringe. Insert the tip and pressurize the cement into each of

the peg holes. Further pressurize the cement using the

Punch, remove the Punch and refill the drill holes with

cement. This will allow for cement pressurization as well as

removal of any excess cement on the glenoid surface.

Attach the appropriately sized Combo Inserter/Extractor to the

corresponding Fin-Lock implant and screw on the Glenoid

Impactor Handle. Apply cement to cover the entire backside of

the Fin-Lock implant and impact the implant construct with a

mallet until there is complete contact between the back side of

the implant and the prepared glenoid surface. It may be

necessary to use the oval Glenoid Impactor to fully seat the

component. Maintain pressure directly on the glenoid

component until the cement has hardened.

6a-8

6a-9

6a-10

6a: Fin-Lock Glenoid System (continued)

6b- 2

Cannulated Drill/Cannulated Reaming

When exposure is deemed adequate, use the Glenoid Sizers and

Glenoid Holder to size the glenoid. Mark the center of the glenoid

using the hole in the Glenoid Sizer with a skin marker. Attach the

appropriately sized Pin Bushing onto the selected size Glenoid

Drill Guide. Align with the center mark, and using the included

2.0mm Guide Pin, drive through the Pin Bushing until adequate

purchase is achieved into the glenoid. If increased retroversion is

noted on preoperative imaging studies, then orient the Glenoid

Drill Guide to correct this retroversion by placing the drill guide in

a plane that is anteverted from the native glenoid plane prior to

Guide Pin insertion. Remove the Drill Guide/Pin Bushing. Attach

the appropriately sized 5-fluted Glenoid Reamer to the Straight

Drill Shaft. Slide over the Guide Pin, start the reamer before

making contact with the bone and ream accordingly until proper

concavity has been achieved and cartilage has been removed. It is

important to remember that over-reaming will both decrease the

surface area of the glenoid face and reduce the depth of the

glenoid vault. Excessive glenoid reaming should be avoided.

Leaving the Guide Wire secure in the bone, use the Cannulated

Peg Drill to create the center hole. Remove the Guide Wire.

Alternative Non-Cannulated Drill/Reaming

When exposure is deemed adequate, use the Glenoid Sizers and

Glenoid Holder to size the glenoid. Also, mark the center of the

glenoid using the hole in the Glenoid Sizer with a skin marker.

Attach the Glenoid Solid Peg Drill onto the Straight Drill Shaft and

use the center hole in the appropriately sized Glenoid Drill Guide.

Drill the central hole. Attach the appropriately sized Glenoid

Reamer to the Straight Drill Shaft.

Insert the nub of the reamer into the central hole. Start the

Reamer before making contact with the bone and ream

accordingly until proper concavity has been achieved and

cartilage has been removed. It is important to remember that

over-reaming will both decrease the surface area of the glenoid

face and reduce the depth of the glenoid vault. Excessive glenoid

reaming should be avoided. Align the Glenoid Drill Guide with the

current center hole and drill using the Peg Drill.

6b- 1

Step 6b • Pegged Glenoid Preparation and Implantation

6b- 1

6b-2

Step 6b • Pegged Glenoid Preparation and Implantation (continued)

Peripheral Peg Drilling

Place an Anti-rotation Peg in the center hole using the

Anti-rotation Peg Holder. This will help stabilize the drill

guide during the drilling of the peripheral peg holes.

Rotate the drill guide to desired orientation and drill the

peripheral peg holes.

After each peripheral peg hole is drilled, insert an Anti-

rotation Peg to maintain alignment of the drill guide. The

preferred scenario is drilling so as not to penetrate the

scapula which will allow you to pressurize the cement

mantle. Check the quality of the glenoid bone

preparation by determining if the component is directly

supported by precisely contoured bone, which should

prevent the component from rocking, even when an

eccentric load is applied to the rim of the implant.

Punch/Trial

A Glenoid Peg Punch is available to check hole

positioning/depth. Check each peripheral hole to

determine whether it penetrates the scapula at its base.

If penetration is detected consider bone grafting the

hole. The Glenoid Peg Punch can be utilized to impact

the graft. Select the appropriate Glenoid Peg Trial and

impact the trial onto the glenoid using the Glenoid

Impactor. The trial matches the drill diameter and will

give you a secure trial fit. Visualize that the trial

component sits flush with the prepared glenoid surface

through the slots in the trial. Remove the trial and

irrigate the glenoid using pulsative lavage to remove

blood and tissue debris from the three drill holes.

Open the appropriately sized pegged glenoid implant. While cement is being prepared, obtain hemostasis by using the

Cement Pressurizer and attaching it to the T-Handle. Hemostasis may also be achieved by packing each of the peg

holes with thrombin and surgical gauze or gel foam. Mix cement using manual or syringe application. The cement is

placed into a 60cc Catheter/Toomey syringe. The end of the syringe is cut with scissors. The tip is inserted, and the

cement pressurized into each of the peg holes. Further pressurize the cement and refill the drill holes with cement. This

will allow for cement pressurization as well as removal of any excess cement on the glenoid surface.

Apply cement to cover the entire backside of the pegged glenoid component, insert the implant, and use the Glenoid

Impactor to seat the component until there is complete contact with the perimeter of the glenoid. Maintain pressure

directly on the glenoid component until the cement has hardened.

6b- 3

6b- 4

6b- 5

Note

The Peg Punch is the same

dimension as the final

implant. Additional cement

must be placed in the

holes after pressurization

or the implant will not be

adequately cemented.

6b- 4

6b- 3

If using the Keeled Glenoid implant, prepare the glenoid

as previously described. As mentioned in Step 6b-1 and

6b-2, size, then drill the central hole and ream the

glenoid. Proceed with drilling the peripheral peg holes.

Use a burr, rongeur or curette to connect the peg holes

for the keel of the prosthesis. Excavate the bone in the

base of the coracoid and down the lateral border of the

scapula to help lock the keeled prosthesis with cement.

Use the Glenoid Keel Punch to impact the bone in the

glenoid fossa for proper fit of the Glenoid Keel Trial. The

Glenoid Keel Trials have slots in them to visualize that

the back of the prosthesis will sit flush on the bone of

the glenoid fossa. Commence with trialing.

Open the appropriately sized keeled glenoid implant.

While cement is being prepared, obtain hemostasis by

packing the keel hole with thrombin and surgical gauze

or gel foam. Mix cement using manual or syringe

application. The cement is placed into a 60cc Catheter/

Toomey syringe. The end of the syringe is cut with

scissors. The tip is inserted, and the cement pressurized

into the keel hole. Further pressurize the cement using

the Glenoid Keel Punch, remove the punch and refill the

keel hole with cement. This will allow for cement

pressurization as well as removal of any excess cement

on the glenoid surface.

Apply cement to cover the entire backside of the keeled

glenoid component, insert the implant, and use the

Glenoid Impactor to seat the component until there is

complete contact with the perimeter of the glenoid.

Maintain pressure directly on the glenoid component

until the cement has hardened.

6c-2

6c- 1

6c- 2

6c- 1

Note

The Keel Punch is the same

dimension as the final

implant. Additional cement

must be placed in the

holes after pressurization

or the implant will not be

adequately cemented.

Step 6c • Keeled Glenoid Preparation and Implantation

7- 2

7- 1

LRG

STD

SML

7 - 2

Step 7 • Humeral Canal Preparation

Side the Depth Stop onto the Stem Trial Handle prior to attaching it to the 6mm

Humeral Stem Trial. Place the tip of the stem trial at the most superior point on

the resected humerus just behind the long head of the biceps groove, so

that it is aligned with and ready to pass directly down the intramedullary canal.

Using the Stem Trial, create a pilot hole and then sequentially trial/impact the

medullary canal in line with its long axis. If the extramedullary cutting guide was

used the Starter Awl can be used to create the pilot hole. Continue sequential

trialing/impacting, following the path created through the intramedullary canal,

increasing the Stem Trial diameter in 1mm increments until a solid fit is achieved

in the humerus.

7 - 1

The laser etching below the hole is for the Small Proximal Body and the etching

above the hole is for the Large Proximal Body. If using a Small or Large body

height, impact until the appropriate laser etching is parallel with the osteotomy.

Tip

With the Stem Trial Handle attached to the stem trial,note the final Stem

Trial diameter. This will determine the size of the final distal stem implant.

When trialling to determining the appropriate body and stem size,

trialling to the Small Body line will allow you up-size during a conversion

to a Reverse.

Note

The diagonal laser markings and hole on the inserter handle correspond to

the depth required for the Small, Standard, and Large Proximal Bodies. If a

depth stop is not available, for the Standard Body, place a 3.2mm Fixation

Pin through the hole and drive the trial down until the pin sits flush on the

osteotomy. Remove the pin and ensure the trial does not advance further. If

trial advances, additional sequential trialing/impacting to a larger diameter

is needed, be sure to stop when resistance within the canal is felt.

9- 1

9- 2

9- 3

9- 1

9- 2

9- 3

Step 9 • Humeral Head Trial

Osteotomy Evaluation/Calcar Reaming

Place the Taper Adaptor onto the Body Trial. Attach the

Trial Calcar Planar onto the ratcheting T-Handle to remove

any excess bone on the surface of the osteotomy

The angle of the Trial Calcar Planar when fixed onto the

Taper Adaptor will be parallel to the standard neckshaft

angle at 135°. Assess its relationship to the resected plane.

If the angle diverges by only a few degrees then the Calcar

Planar can be used to finalize the plane.

Note

Ensure all boney protrusions are clear before moving

on to head trialing.

Osteotomy Sizing Template

Select the Head Sizing Plate that most closely covers the

cut surface of the humeral osteotomy.

After determining the diameter of the measured humeral

head, use the Head Sizing Plate to determine if a

concentric or eccentric head is necessary.

Select the appropriately sized Humeral Head Trial.

8 - 1

Step 8 • Body And Stem Trial Insertion

Remove the Stem Trial and attach it to the closest

corresponding Body Trial. Proximal Bodies are interchangeable

and can be used with all stem sizes. If the Trial Stem is

between Proximal Body sizes, it is suggested to start with the

smaller diameter Body Trial and go up to the larger diameter

Body Trial if needed. Attach the Body/Stem Trial construct to

the Humeral Trial Inserter/Extractor inserting the D feature in

the taper hole for alignment, then tightening the top of the

Humeral Trial Inserter/Extractor until the Body/Stem Trial is

secure.

Using the Cutting Template Handle for a threaded version rod

on the Humeral Trial Inserter/Extractor (which is set at 30° of

retroversion), impact the stem in the correct retroversion,

which corresponds to the version set during the humeral head

osteotomy. Seat the Body/Stem Trial until the Humeral Trial Inserter/Extractor sits on the resected surface.

At this point, the Body Trial is seated flush to the resection. Remove the Humeral Trial Inserter/Extractor.

30°

Step 8 • Body And Stem Trial Insertion

9-4b

Note

If the Humeral Head Trial does not lock onto the

Taper

Adaptor, it may be necessary to Calcar plane further to

clear any boney impingement.

Eccentric Head Trialing

If the Stem Trial is off-center in relation to the humeral

osteotomy, the Eccentric Head Trial will allow the head to

be rotated into the head position that allows maximum

coverage of the proximal humerus.

Place the Eccentric Head Trial onto the Taper Adaptor on

the Body Trial and rotate the head trial to the desired

position. Once the Eccentric Head Trial position is selected,

lock the Head Trial position with the Head Impactor. Mark

the final position of the Eccentric Head Trial peripheral

notch on the humeral surface for later reference with the

final implant.

Ensure the taper adapter remains in the head for proper

eccentricity assessment if using the back table assembly

technique.

Head Trialing

This system measures its humeral heads using a base

width x height measurement. A 46x17 head is 46mm wide x

17mm tall. This makes different spherical radii in one base

width as height changes. Some systems use a spherical

diameter measurement which keeps a constant spherical

radii, yet this causes the base width to change as height

changes. With this system, you choose the diameter that

best fits your osteotomy, then choose the head height that

best matches the glenoid component while allowing for

adequate soft tissue balancing.

9- 4

9- 4a

9- 4b

Concentric Head Trialing

Once trial is selected, place the Concentric Head Trial

onto the Taper Adapter on the Body Trial. Check that the

head trial achieves appropriate coverage of cortical bone,

with 5-8mm height above the greater tuberosity. Proper

head thickness can be determined during trial reduction. If

necessary, increase or decrease selected head size/type and

reassess in place. A final decision will be made during trial

reduction, with the glenoid component in place.

Spherical Diameter vs. Base Width Diameter

(Drawings are not actual size)

Spherical Diameters:

base width changes

with each height Base Width Diameters:

base width same for each height

48mm

Titan Base Width Diameter Sizing:

48-15 / 48-18 / 48-21

21 mm 18 mm 15 mm

48mm

Spherical Diameter Sizing:

48-15 / 48-18 / 48-21

43.5mm

45.5mm

46.5mm

21mm

18mm

15mm

9- 4

12- 1

Step 11 • Preparation for Repair of Subscapularis Tendon

If the subscapularis tendon was removed with a small portion of lesser

tuberosity, two permanent sutures are passed through two sets of holes for

later tension band suturing of the lesser tuberosity fragment to its native

bed. In this circumstance, we recommend placing the sutures through the

suture holes and/or around the stem of the prosthesis and pulling the slack

out of the sutures just before the prosthesis is placed into its final seated

position within the humeral canal.

If the subscapularis tendon was cut using sharp dissection a tendon to

tendon repair can be performed after final prosthesis has been implanted.

Step 12 • Body and Stem Implant Assembly

Proximal Body and Distal Stem Assembly

Select and remove from their packaging the final Humeral Body and

Humeral Stem sizes that correspond to the trials. Seat and secure the

Humeral Body implant onto the Stem Impaction Stand. Place the

Humeral Stem implant onto the Humeral Body with finger pressure.

Place the Stem Impactor over the tip of the humeral stem and engage

the tapers with a few mallet strikes.

11- 1

12- 1

10- 1

10 - 2

Step 10 • Soft Tissue Balancing and Trial Removal

With the Body/Stem Trial and Humeral Head Trial in place, use a burr or a

rongeur to remove any residual osteophytes extending beyond the

periphery of the humeral head. It is important to balance soft tissue tension

with the appropriate trial humeral head in place. It should be possible to

fully internally rotate the arm across the chest so that the hand of the

involved shoulder easily rests on top of the opposite shoulder, without

elevating the involved shoulder off the table. It should also be possible to

externally rotate the arm 30-40° and still re-approximate the subscapularis

tendons to the cut surface of the neck of the humerus. With the arm in

neutral rotation, the humeral head should posteriorly sublux 50%

or more but should spontaneously reduce when the posterior force is

released. Remove the Head Trial/Taper Adapter construct by hand.

If difficult to remove use the Head Extractor tool under the trial head.

Stem Trial Removal

Mark the osteotomy in line with the laser etching on the back of the Body

Trial. This will be used as a reference for matching rotation with the final

implant. Extract Body/Stem Trial construct from the humeral canal using

the Threaded T-Handle or Humeral Trial Inserter/Extractor and Slotted

Mallet.

10 - 2

10- 1

Step 12 • Body and Stem Implant Assembly (continued)

13- 1

Stem Insertion

Insert the assembled Body/Stem implant into the prepared

humerus using the Humeral Implant Inserter/ Extractor. Use

the Head Cutting Template Handle / Version Rod on the

Humeral Implant Inserter/Extractor to set the stem in the

correct anatomic retroversion, which should match the

version set at the time of the humeral osteotomy and

trialing. The body has a laser mark that can be lined up with

the previous mark placed on the osteotomy. Slowly impact

the implant and stop once the stem is firmly seated and the

top of the body is approximately 2-4mm above the

osteotomy. This will ensure Morse taper assembly with

Humeral Head.

If desired, use the gold Implant Calcar Planar to remove any

excess bone at the osteotomy.

Note

Thoroughly clean and dry both tapers to ensure

proper fit.

12- 2 12- 2

Remove the Humeral Body Screw from its packaging

and insert into the Humeral Body with the Driver Handle,

Torque Limiter and 1/8 Hex Driver. Tighten the screw until

the torque limiter clicks.

Note

The implant stand can be used to hold the implant

while tightening the Humeral Body Screw.

The torque

limiter is designed to tighten the screw to 2 Nm.

Step 13 • Stem/Body Implantation and In-Situ Head Assembly

This system is designed as a press-fit prosthesis, in which the press-fit is achieved via the tapering and splines of the

distal stem. The use of cement is not necessary or recommended. Cemented stems are available for cases

in which a press-fit stem would not be appropriate.

13 - 1

Step 1: Impact directly

in line with the

taper to lock.

135°

Step 2: Final implant

seating – impact

directly in line with

taper to ensure loc

13- 2

13- 3

13- 2

Humeral Head Assembly

In–Situ

Place the selected Humeral Head onto the clean and dry Morse

taper. If using an Eccentric Humeral Head you can place a

mark on the articular surface of the Humeral Head reflecting

the eccentric etching on the bottom of the Humeral Head. This

will allow you to line up the mark on the head with the

previously recorded position on the osteotomy. Once Humeral

Head position is satisfactory, impact the head in line with

the taper using the Head Impactor.

Note

The implant must be seated by impacting the head

in line with the taper.

Remove any further osteophytes. The Humeral Head should be about 5mm above the top of the greater tuberosity. If a

lesser tuberosity osteotomy was performed, there is often a portion of the anterior part of the humeral prosthesis that

overhangs the bone. This is where the lesser tuberosity is going to fit. Now perform the final checks for range of motion,

correct version and stability.

Note

Once secured, check the humeral head by hand to confirm

taper lock.

Back Table Assembly Option

Seating the Standard/Concentric Humeral Head

With the Humeral Body/Stem prosthesis in the stand, the proximal plane of the proximal body will be parallel to the

table top and allow the final humeral head to be driven down perpendicular to the table top, ensuring proper seating of

the Morse taper. With the final head in place, impact it into the Humeral Body using the rubber tipped Head Impactor

and the Slotted Mallet. Impact the head 3-4 times to ensure proper seating and Morse taper.

Seating the Eccentric Humeral Head

There is an etching on the nonarticular surface of the final Eccentric Humeral Head that corresponds to the peripheral

slot on the Eccentric Head Trial. Line the etching up to the referenced position previously marked on the Head

Impaction Stand. It may be helpful to use a skin marker to place a mark on the articular surface near the etching. This

technique ensures that the final prosthesis will have the same orientation as the Trial construct. Firmly impact the head

by placing the rubber tipped Head Impactor on the Humeral Head and striking the impactor three to four times with the

Slotted Mallet.

Insertion of Final Humeral Head, Body and Stem Assembly

Place the final assembled Humeral Head/Body/Stem down the humeral canal checking rotation as it is seated. Use the

Head Impactor to insert the assembly to the final seated position. The Humeral Head should sit flush on the osteotomy.

Remove any further osteophytes. The Humeral Head should be about 5 mm above the top of the greater tuberosity. If a

lesser tuberosity osteotomy was performed there is often a portion of the anterior part of the humeral prosthesis that

overhangs the bone. This is where the lesser tuberosity is going to fit. Now perform the final checks for range of

motion, correct version and stability.

Step 13 • Stem/Body Implantation and In-Situ Head Assembly (continued)

Long Stem Option and Implantation

The surgical technique for implanting a Titan Modular Shoulder System Long Stem differs slightly from the standard stem

process.

Long Stem Trialing

Attach the T-Handle to the Starter Awl and create a 6mm pilot hole in the humerus. Continue progressively reaming using

cylindrical reamers of increasing diameter to 8, 10, or 12mm in either the 125mm or 165mm stem length options. The canal is

reamed until cortical chatter is present and inserted to the depth of the laser mark associated with the desired height of humeral

body.

It is important to prepare the medullary canal over its total length. The final reamer used will correlate to the proper Trial Long

Stem selected. The reamer, trial, and implant are line to line; minimizing cement to the stem flutes and within the surrounding

trabecular bone.

Removing the Humeral Head

The Humeral Head can be removed using the Humeral Head Extractor. Place the two

prongs of the extractor between the humeral head and the osteotomy surface so

that the prongs will advance in each side of the linking component. Lift the head off

the proximal humeral body taper by impacting the end of the extractor with the

slotted mallet.

Removing the Stem

The stem is designed to remain in the humeral canal in a revision or conversion to

reverse. If removing the Stem is necessary, leave the Humeral Body on and the Body

Screw fully inserted. Insert the Implant Inserter/Extractor over the taper and use the

slotted mallet against the strike plate until the stem and body are removed from the

bone intact. It is recommended to also have the Titan Modular Shoulder System

Long Stem tray available and use the stem adapter with the slap hammer.

Removing only the Proximal Humeral Body

The Humeral Body can be removed using the T-Handle and the final Implant

Inserter/ Extractor. First disengage the Humeral Body Screw and remove using the

1/8 Hex Driver. Unthread the inner rod from the Implant Inserter/Extractor and

replace with the T-Handle. Place the Inserter/Extractor over the taper, and thread

the T-Handle into the Humeral Body until resistance is felt. Grip the Inserter/

Extractor firmly to control rotation of implant and continue to tighten the T-Handle

to disengage the Morse taper between the Humeral Body and distal stem. Remove

the Humeral Body, which will be threaded onto the T-Handle.

Step 14 • Revision Procedure

Removal of the humeral head and/or proximal humeral body during revision surgery

can be achieved without disturbing a well-fixed distal stem.

14- 1

14- 2

14- 1

14- 2

14- 3

Note

Long stems are intended for cemented use only

The Long Stem Reamers, within the Long Stem instrument set, are a special order item and do not come with the standard

TSS and RSS instrumentation set

If a greater cement mantle is desired, choose a Long Stem Implant diameter smaller than the reamer and Trial Long Stem

diameter used for preparation.

Humeral Body Trial

Attach the selected Body Trial/Long Stem Trial construct to the Humeral Trial Inserter/Extractor by inserting the D feature in the

taper hole for alignment. Tighten the top of the Humeral Trial Inserter/Extractor knob until the selected Body Trial/Long Stem

Trial construct is secure.

Affix the Cutting Template Handle / Version Rod to the Humeral Trial Inserter/Extractor to ensure proper version. The Cutting

Template Handle / Version Rod is aligned parallel with the patient’s forearm and initially sets the trial construct in 30° of

retroversion. Using the Slotted Mallet, carefully drive the Body Trial/Long Stem Trial into the proximal humerus so that it is in

line with the long axis. Seat the Body Trial/ Long Stem Trial until the desired fit is achieved.

The Body Trial/Long Stem Trial should be positioned at the correct height to preserve the anatomic reconstruction. If the

desired Body Trial size is between the available options after the appropriate Long Stem Trial has been determined, its

suggested to start with the smaller height/diameter Body Trial and go up to the larger height/diameter Body Trial if needed.

Humeral Body and Long Stem Implant Assembly

Remove the final Humeral Body and Long Stem implants that correspond to the trials from their packaging. Seat and secure

the selected Body Implant onto the Stem Impaction Stand. Place the Long Stem Implant onto the Humeral Body with finger

pressure. Place the Stem Impactor over the tip of the humeral stem and engage the tapers with a few mallet strikes. Then

insert the body screw using the 1/8 Hex Driver, attached to the Torque Limiter. Once the Body/Stem construct is secure, place

the selected Humeral Head implant onto the clean and dry Morse taper. Impact the head in line with the taper using the Head

Impactor with a few strikes of a mallet.

Cementing the Stem

Thoroughly irrigate the medullary canal to remove debris. Use either a small piece of cancellous bone or utilize a cement

restrictor and place 1-2 cm below distal stem to prevent cement from extruding to the elbow. Use either medium or high

viscosity cement, place cement down the humeral canal using finger pressure. Now insert the full implant construct.

Note

The Primary Body Trials from the Total Shoulder System Humeral Tray 1 can be used with the Trial Long Stems to determine

proper prosthesis height prior to cementing.

Note

For further instructions, please refer to:

Step 9 – Humeral Head Trialing

Step 10 – Soft Tissue Balancing

Long Stem Option and Implantation (continued)

Once final implant is in place, the subscapularis tendon repair can be completed with the previously placed sutures.

When necessary, perform a biceps tenodesis prior to wound closure.

Thoroughly irrigate the wound with antibiotic solution. If a regional anesthetic is not used then infiltrate the soft tissue

with a local anesthetic that will last 6-8 hours. A wound drainage system is recommended to prevent formations of

postoperative hematoma.

The wound may be closed according to surgeon preference. Careful attention to wound closure will result in a

cosmetically acceptable incision. After the dressing and shoulder immobilizer are in place, the use of a cold wrap is

recommended. This prefrozen wrap can be placed on the shoulder in the operating room and replaced with another unit

every three hours. The combination of regional anesthetic or local anesthetic and the immediate cooling seems to

decrease the amount of postoperative pain.

Step 15 • Wound Closure

The patient is placed in a comfortable immobilizer with arm at their side and regional block analgesia as preferred.

Active pendulum exercises are not encouraged in order to prevent stretch of the anterior repair. However, supine

passive range of motion within 24-72 hours of surgery is of the utmost importance. The limits to the extent of passive

range of motion performed should not exceed the safe zone of rotation observed at surgery after subscapularis closure.

Supervised physical therapy program is recommended after 24-48 hours. Supervised active assisted and passive range of

motion mobilization is suggested for the first 72 hours. Active assisted and passive assistance is recommended for 6

weeks after which terminal stretching and active range of motion is initiated. Home pulley system is initiated at 72

hours.

The sling immobilizer may be abandoned at approximately 6 weeks to protect the subscapularis repair. Most patients

are able to perform all their exercises at home in a physician supervised therapy program. Supervision of all post-

operative therapy is recommended. Therapy should be individualized and based on the status of the repaired tissues and

muscle strength. Most importantly, protection of the subscapularis repair and/or rotator cuff repair will dictate the

amount of stretching or resistance as well as the duration of immobilization. Progressive resistance for the rotator cuff

including the subscapularis is initiated at 10-12 weeks depending on the quality of rotator cuff tissue and of the repair.

Guarded loading of the shoulder should be observed for the first 4-6 months post-operatively. Complete recovery from

surgery generally occurs at 9-12 months.

Postoperative Therapy Protocol

Humeral Tray 1: Base

1. Stem Trial Handles

2. Trial Calcar Planer

3. Trial Osteotomy Cover

4. Canal Osteotomy Cover

5. Total Shoulder Depth Stops

6. Humeral Stem Trials

7. Humeral Trial Inserter/Extractor

8. Humeral Body Trials

9. Taper Adaptors

10. Locking Body Screws

11. Fracture Body Trials

Reference ReferenceDescription DescriptionQTY QTYNo. No.

CSA-000-14

HDL-0920-043-001

RMR-0923-050-002

CVR-0920-076L

CVR-0920-076S

CVR-0920-077L

CVR-0920-077S

HDS-0920-069-001

TRL-0920-025-06

TRL-0920-025-07

TRL-0920-025-08

TRL-0920-025-09

TRL-0920-025-10

TRL-0920-025-11

TRL-0920-025-12

TRL-0920-025-13

TRL-0920-025-14

TRL-0920-025-15

TRL-0920-025-16

INS-0923-046-001

TRL-0920-020-08STD

TRL-0920-020-10LRG

TRL-0920-020-10SML

TRL-0920-020-10STD

TRL-0920-020-12STD

TRL-0920-020-14LRG

TRL-0920-020-14SML

TRL-0920-020-14STD

ADT-0923-065-001

BSW-0920-01NS

TRL-0923-021-08LRG

TRL-0923-021-08SML

TRL-0923-021-08STD

Generic Case Lid – Full DIN

Stem Trial Handle

TSS Trial Calcar Planer, 2.5

Trial Osteotomy Cover, Large

Trial Osteotomy Cover, Small

Canal Osteotomy Cover, Large

Canal Osteotomy Cover, Small

Depth Stop

Humeral Stem Trial, 6mm

Humeral Stem Trial, 7mm

Humeral Stem Trial, 8mm

Humeral Stem Trial, 9mm

Humeral Stem Trial, 10mm

Humeral Stem Trial, 11mm

Humeral Stem Trial, 12mm

Humeral Stem Trial, 13mm

Humeral Stem Trial, 14mm

Humeral Stem Trial, 15mm

Humeral Stem Trial, 16mm

TSS Trial Inserter/Extractor, 2.5

Body Trial, 8 Standard

Body Trial, 10 Large

Body Trial, 10 Smal

Body Trial, 10 Standard

Body Trial, 12 Standard

Body Trial, 14 Large

Body Trial, 14 Small

Body Trial, 14 Standard

TSS Taper Adapter, 2.5

Locking Body Screw

TSS Fracture Body Trial Lrg, 2.5

TSS Fracture Body Trial Sml, 2.5

TSS Fracture Body Trial Std, 2.5

1. Head Resection Guide

2. Head Cuing Templates

3. Head Cuing Depth Gauge

4. Body/Stem Impactor

5. Version Rods

6. Pin Puller

7. Fixation Pin

8. Torque Limiter

9. Hex Driver

10. Cuing Template Handle

11. Head Sizing Templates

12. Sloed Mallot

13. Starter Awl

14. Driver Handle

15. Quick Connect Ratchet Handle

Humeral Tray 1: Insert

SET189-A001 Head Cuing Guide 1

TMP-0920-040-001L Head Cuing Template, Le 1

TMP-0920-040-001R Head Cuing Template, Right 1

GAU-0920-058-001 Head Cuing Depth Gauge 1

IMP-0920-055-001 Stem Impactor 1

SET189-D007 Version Rod 1

PUL-0920-087-01 Pin Puller 1

PIN-0920-051-001 Fixation Pin 2

TRQ-0920-086-01 Torque Limiter 1

SCR-0920-060-001 1/8 Hexdriver 1

ROD-0923-040-001 TSS Head Cuing Template Rod, 2.5 1

MAL-0920-085-01 Sloed Mallet 1

AWL-0920-042-001 Starter Awl 1

G107992_B Driver Handle w/ Sm AO 1

HSG-0920-041-001 Head Sizing Gauge 38-46 1

HSG-0920-041-002 Head Sizing Gauge 48-52 1

NR135004-J-004 T-Handle w/ Lg AO or Quick Connect Ratchet T-Handle

Reference Description QTY

No.

Humeral Tray 2: Base

1. Head Extractor

2. Body Separator

3. Humeral Implant Inserter/Extractor

4. Implant Calcar Planer

5. Head Impaction Stand Inserts

6. Head Impaction Stand Base Assembly

7. Stem Impaction Stand

SET188-A001 Head Extractor 1

SEP-0920-068-001 Body Separator 1

INS-0923-045-001 TSS Implant Inserter/Extractor, 2.5 1

RMR-0923-050-001 TSS Implant Calcar Planer, 2.5 1

INS-0920-071-LRG Head Impaction Stand Insert, Large 1

INS-0920-071-SML Head Impaction Stand Insert, Small 1

INS-0920-071-STD Head Impaction Stand Insert, Std. 1

STD-0920-071-001 Head Impaction Stand, Base Assembly 1

SIS-0920-054-001 Stem Impaction Stand 1

Reference Description QTYNo.

Humeral Tray 2: Insert

1. Head Impactor

2. Taper Disassembly Tool

3. Humeral Head Sizing Plate

4. Humeral Head Trails

234

IMP-0920-079-501 TSS Head Impactor

TDT-0920-044-001 Taper Disassembly Tool

HSP-0923-070-001E TSS Head Sizing Plates 38-40, 2.5 - 38E

HSP-0923-070-002E TSS Head Sizing Plates 38-40, 2.5 - 40E

HSP-0923-070-003 TSS Head Sizing Plates 42-52, 2.5 - 42

HSP-0923-070-004 TSS Head Sizing Plates 42-52, 2.5 - 44

HSP-0923-070-005 TSS Head Sizing Plates 42-52, 2.5 - 46

HSP-0923-070-006 TSS Head Sizing Plates 42-52, 2.5 - 48

HSP-0923-070-007 TSS Head Sizing Plates 42-52, 2.5 - 50

HSP-0923-070-008 TSS Head Sizing Plates 42-52, 2.5 - 52

TRL-0923-010-3814E TSS Head Trial Eccentric, 2.5 38x14mm

TRL-0923-010-4015E TSS Head Trial Eccentric, 2.5 40x15mm

TRL-0923-010-4216C TSS Head Trial Concentric, 2.5 42x16mm

TRL-0923-010-4216E TSS Head Trial Eccentric, 2.5 42x16mm

TRL-0923-010-4416C TSS Head Trial Concentric, 2.5 44x16mm

TRL-0923-010-4416E TSS Head Trial Eccentric, 2.5 44x16mm

TRL-0923-010-4419C TSS Head Trial Concentric, 2.5 44x19mm

TRL-0923-010-4419E TSS Head Trial Eccentric, 2.5 44x19mm

TRL-0923-010-4614C TSS Head Trial Concentric, 2.5 46x14mm

TRL-0923-010-4614E TSS Head Trial Eccentric, 2.5 46x14mm

TRL-0923-010-4617C TSS Head Trial Concentric, 2.5 46x17mm

TRL-0923-010-4617E TSS Head Trial Eccentric, 2.5 46x17mm

TRL-0923-010-4620C TSS Head Trial Concentric, 2.5 46x20mm

TRL-0923-010-4620E TSS Head Trial Eccentric, 2.5 46x20mm

TRL-0923-010-4815C TSS Head Trial Concentric, 2.5 48x15mm

TRL-0923-010-4815E TSS Head Trial Eccentric, 2.5 48x15mm

TRL-0923-010-4818C TSS Head Trial Concentric, 2.5 48x18mm

TRL-0923-010-4818E TSS Head Trial Eccentric, 2.5 48x18mm

TRL-0923-010-4821C TSS Head Trial Concentric, 2.5 48x21mm

TRL-0923-010-4821E TSS Head Trial Eccentric, 2.5 48x21mm

TRL-0923-010-5019C TSS Head Trial Concentric, 2.5 50x19mm

TRL-0923-010-5019E TSS Head Trial Eccentric, 2.5 50x19mm

TRL-0923-010-5022C TSS Head Trial Concentric, 2.5 50x22mm

TRL-0923-010-5022E TSS Head Trial Eccentric, 2.5 50x22mm

TRL-0923-010-5220C TSS Head Trial Concentric, 2.5 52x20mm

TRL-0923-010-5220E TSS Head Trial Eccentric, 2.5 52x20mm

Reference ReferenceDescription DescriptionQTY QTYNo. No.

1. Glenoid Impactor

2. Straight Drill Sha

3. Cement Pressurizer

4. Glenoid Keeled Punches

5. Glenoid Peg Punches

QTY

Pegged/Keeled Glenoid Tray: Base

AREA TO REMAIN OPEN DURING REPROCESSING

IMP-0920-064-001 Glenoid Impactor 1

HDL-0922-082-01 Glenoid Drill Sha 2

PRS-0923-073-001 Pressurizer xsm/s 1

PRS-0923-073-002 Pressurizer m/l 1

PUN-0920-062-001 Glenoid Keel Punch, XSm/Sm 1

PUN-0920-062-002 Glenoid Keel Punch, Med/Lg 1

PUN-0920-072-001 Glenoid Peg Punch, XSm/Sm 1

PUN-0920-072-002 Glenoid Peg Punch, Med/Lg 1

Reference Description QTYNo.

Glenoid Tray: Insert

1. Glenoid Sizers

2. Glenoid Peg Trials

3. Glenoid Keeled Trials

4. Glenoid Reamers

5. Guide Pins

6. Glenoid Drill Guides

7. Glenoid Trial Holder /

Anti-Rotation Peg Holder

8. Cannulated Center Starter Drill

9. Anti-Rotation Pegs

10. TSS Glenoid Solid Peg Drill

11. Pin Bushings

12. Cannulated Peg Drills

1 8

3 5 6 7

SZR-0920-052-000 Glenoid Sizer, Extra Small

SZR-0920-052-001 Glenoid Sizer, Small

SZR-0920-052-002 Glenoid Sizer, Medium

SZR-0920-052-003 Glenoid Sizer, Large

TRL-0920-030-00P Glenoid, Peg Trial, Extra Small

TRL-0920-030-01P Glenoid, Peg Trial, Small

TRL-0920-030-02P Glenoid, Peg Trial, Medium

TRL-0920-030-03P Glenoid, Peg Trial, Large

TRL-0920-030-00K Glenoid, Keel Trial, Extra Small

TRL-0920-030-01K Glenoid, Keel Trial, Small

TRL-0920-030-02K Glenoid, Keel Trial, Medium

TRL-0920-030-03K Glenoid, Keel Trial, Large

RMR-0920-057-000 Glenoid Reamer, Extra Small

RMR-0920-057-001 Glenoid Reamer, Small

RMR-0920-057-002 Glenoid Reamer, Medium

RMR-0920-057-003 Glenoid Reamer, Large

RMR-0920-059-000 Glenoid Five Flute Reamer, XS

RMR-0920-059-001 Glenoid Five Flute Reamer, S

RMR-0920-059-002 Glenoid Five Flute Reamer, M

RMR-0920-059-003 Glenoid Five Flute Reamer, L

GDW-0920-061-501 2.0mm x 150mm Guide Pin

DRG-0922-067-01 Glenoid Drill Guide, X-Sm/Sm

DRG-0922-067-02 Glenoid Drill Guide, Med/Lg

HDL-0920-075-001 Anti-rotation Peg Holder

HDR-0920-063-001 Glenoid Holder

DRL-0920-047-001 Cannulated Center Starter Drill

PEG-0922-074-02 TSS Anti-rotation Peg

DRL-0922-080-01 TSS Glenoid Solid Peg Drill

BSH-0923-048-001 Pin Bushing XS/S

BSH-0923-048-002 Pin Bushing M/L

DRL-0923-047-001 Cannulated Peg Drill

Reference ReferenceDescription DescriptionQTY QTYNo. No.

QTY

Fin-Lock Glenoid Tray: Base

1. Glenoid Punch

2. Fin-Lock Trials

3. Hudson T-Handle

4. Combo Inserter/Impactors

5. Glenoid Impactor

6. 2.8mm Drill Sha

7. Anti-Rotation Peg Holder

8. Glenoid Holder

9. Bowtie Reamer Caddy

(ordered separately)

10. Glenoid Handle

PN-0926-001 Punch 1

TRL-0926-030-00A Trial, Fin-Lock Glenoid, XS 1

TRL-0926-030-01A Trial, Fin-Lock Glenoid, S 1

TRL-0926-030-02A Trial, Fin-Lock Glenoid, M 1

TRL-0926-030-03A Trial, Fin-Lock Glenoid, L 1

HDL-0926-002 Hudson T-Handle 1

IMP-0926-030-00A Combo Inserter/Impactor, XS 1

IMP-0926-030-01A Combo Inserter/Impactor, S 1

IMP-0926-030-02A Combo Inserter/Impactor, M 1

IMP-0926-030-03A Combo Inserter/Impactor, L 1

IMP-0920-064-001 Glenoid Impactor 1

DRS-0926-001 2.8mm Drill Sha 2

HDL-0920-075-001 Anti-Rotation Peg Holder 1

HDR-0940-048-001 Glenoid Holder 1

RMR-0926-00BC Cannulated Bowtie Reamer, XS 1

RMR-0926-01BC Cannulated Bowtie Reamer, S 1

RMR-0926-02BC Cannulated Bowtie Reamer, M 1

RMR-0926-03BC Cannulated Bowtie Reamer, L 1

RMR-0926-00BN Noncannulated Bowtie Reamer, XS 1

RMR-0926-01BN Noncannulated Bowtie Reamer, S 1

RMR-0926-02BN Noncannulated Bowtie Reamer, M 1

RMR-0926-03BN Noncannulated Bowtie Reamer, L 1

IMH-0926-000 Glenoid Impactor Handle 1

Reference ReferenceDescription DescriptionQTY QTYNo. No.

Fin-Lock Glenoid Tray: Insert

1. Fin-Lock Sizers

2. Five Fluted Glenoid Reamers

3. 2.8mm Guide Wire

4. Glenoid Drill Caddy

5. Angled Handle

6. Fin-Lock Modular Drill Guide

7. Self-Retaining Drill Adaptor

8. Fin-Lock Starter Drill Guides

SZR-0926-030-000 Sizer, Fin-Lock Glenoid, XS

SZR-0926-030-010 Sizer, Fin-Lock Glenoid, S

SZR-0926-030-020 Sizer, Fin-Lock Glenoid, M

SZR-0926-030-030 Sizer, Fin-Lock Glenoid, L

SZR-0926-030-003 Sizer, Fin-Lock Glenoid, XS, +3

SZR-0926-030-013 Sizer, Fin-Lock Glenoid, S, +3

SZR-0926-030-023 Sizer, Fin-Lock Glenoid, M, +3

SZR-0926-030-033 Sizer, Fin-Lock Glenoid, L, +3

SZR-0926-030-005 Sizer, Fin-Lock Glenoid, XS, +5

SZR-0926-030-015 Sizer, Fin-Lock Glenoid, S, +5

SZR-0926-030-025 Sizer, Fin-Lock Glenoid, M, +5

SZR-0926-030-035 Sizer, Fin-Lock Glenoid, L, +5

RMR-0926-00C Cannulated Reamer, XS

RMR-0926-01C Cannulated Reamer, S

RMR-0926-02C Cannulated Reamer, M

RMR-0926-03C Cannulated Reamer, L

RMR-0926-00N Non-Cannulated Reamer, XS

RMR-0926-01N Non-Cannulated Reamer, S

RMR-0926-02N Non-Cannulated Reamer, M

RMR-0926-03N Non-Cannulated Reamer, L

GDW-0926-001 2.8mm Guidewire

DRL-0926-015-S Drill, Central Peg, 15mm, Solid

DRL-0926-018-S Drill, Central Peg, 18mm, Solid

DRL-0926-015-C Drill, Central Peg, 15mm, Cannulated

DRL-0926-018-C Drill, Central Peg, 18mm, Cannulated

DRL-0926-001 Starter Drill

DRL-0926-002 Peripheral Drill

PEG-0926-000 Central Anti-rotation Peg

HDL-0926-001 Angled Handle

DRG-0926-001 Fin-Lock Drill Guide

ADP-0980-105-00 Self-retaining Drill Adaptor

DRG-0926-002 Starter Drill Guide, XS/S

DRG-0926-003 Starter Drill Guide, M/L

Reference ReferenceDescription DescriptionQTY QTYNo. No.

1 Reamers

2 Slap Hammer

3 Adapters

Cemented Long Stem Base

QTY

RMR-0950-025-08125 Reamer Cemented Long Stem, 8mm x 125mm 1

RMR-0950-025-10125 Reamer Cemented Long Stem, 10mm x 125mm 1

RMR-0950-025-12125 Reamer Cemented Long Stem, 12mm x 125mm 1

RMR-0950-025-08165 Reamer Cemented Long Stem, 8mm x 165mm 1

RMR-0950-025-10165 Reamer Cemented Long Stem, 10mm x 165mm 1

RMR-0950-025-12165 Reamer Cemented Long Stem, 12mm x 165mm 1

SLP-1002-519 Slap Adaptor 1

ADA-0950-040-501 Trial Adaptor 1

ADA-0950-040-502 Stem Adaptor 1

Catalog No. Description QTYNo.

Cemented Long Stem Insert

1 Trial Cemented Long Stems

2 Deﬁnitive Stem Primary Body Trials

AREA TO REMAIN OPEN

DURING REPROCESSING

TRL-0950-025-08125 Trial Cemented Long Stem, 8mm x 125mm 1

TRL-0950-025-10125 Trial Cemented Long Stem, 10mm x 125mm 1

TRL-0950-025-12125 Trial Cemented Long Stem, 12mm x 125mm 1

TRL-0950-025-18165 Trial Cemented Long Stem, 8mm x 165mm 1

TRL-0950-025-10165 Trial Cemented Long Stem, 10mm x 165mm 1

TRL-0950-025-12165 Trial Cemented Long Stem, 12mm x 165mm 1

TRL-0920-120-08STD Deﬁnitive Stem Primary Body Trial - 08 Std 1

TRL-0920-120-10SML Deﬁnitive Stem Primary Body Trial - 10 Sml 1

TRL-0920-120-10STD Deﬁnitive Stem Primary Body Trial - 10 Std 1

TRL-0920-120-10LRG Deﬁnitive Stem Primary Body Trial - 10 Lrg 1

TRL-0920-120-12STD Deﬁnitive Stem Primary Body Trial - 12 Std 1

TRL-0920-120-14SML Deﬁnitive Stem Primary Body Trial - 14 Sml 1

TRL-0920-120-14STD Deﬁnitive Stem Primary Body Trial - 14 Std 1

TRL-0920-120-14LRG Deﬁnitive Stem Primary Body Trial - 14 Lrg 1

TRL-0923-121-08SML Deﬁnitive Stem Fracture Body Trial - 2.5 Sml 1

TRL-0923-121-08STD Deﬁnitive Stem Fracture Body Trial - 2.5 Std 1

TRL-0923-121-08LRG Deﬁnitive Stem Fracture Body Trial - 2.5 Lrg 1

Catalog No. Description QTYNo.

Titan Modular Shoulder Instrumentation

Retractor Tray

1. Fukuda Retractors

2. Darrach Retractors

3. Deltoid Retractor

4. Curved Hohmann Retractors

5. Kolbel Retractor Frame

6. Kolbel Retractor Blades –

Small, Large, Extra Large

7. Spiked Glenoid Retractors

RET-920-50S

RET-920-50L

RET-920-11

SRET-920-11L

RET-920-20

RET-920-31

RET-920-60

RET-920-61S

RET-920-61L

RET-920-61XL

RET-920-41S

RET-920-41L

Catalog No. Description QTYNo.

Fukuda Retractor-Small

Fukuda Retractor-Large

Darrach Retractor-Small

Darrach Retractor-Large

Deltoid Retractor-Large

Hohman Retractor

Kolbel Retractor Frame

Kolbel Retractor-Small

Kolbel Retractor-Large

Kolbel Retractor-XLarge

Glenoid Retractor-Small

Glenoid Retractor-Large

Ordering Information and Implant Dimensions

Length

Press-Fit Stem Dimensions (mm), Ti

Diameter A Diameter B Diameter C

A B C

Primary Body Dimensions (mm), Ti

Base Diameter

Height

Trunnion

Offset

Max Length

Max Width

Cemented Stem Dimensions (mm), CoCr

Spherical Diameter Ø

Humeral Head Dimensions (mm), CoCr

Height

Width

Humeral Head Spherical Offset

Catalog Number Height Width Diameter Ø (Eccentric) Concentric

MHH-0923-010-3814X 14 38 41 2.5 No Option

MHH-0923-010-4015X 15 40 43 2.5 No Option

MHH-0923-010-4216X 16 42 45 4 C

MHH-0923-010-4416X 16 44 48 4 C

MHH-0923-010-4419X 19 44 45 4 C

MHH-0923-010-4614X 14 46 54 4 C

MHH-0923-010-4617X 17 46 49 4 C

MHH-0923-010-4620X 20 46 47 4 C

MHH-0923-010-4815X 15 48 56 4 C

MHH-0923-010-4818X 18 48 51 4 C

MHH-0923-010-4821X 21 48 49 4 C

MHH-0923-010-5019X 19 50 53 4 C

MHH-0923-010-5022X 22 50 51 4 C

MHH-0923-010-5220X 20 52 55 4 C

Cemented Stem Diameter Diameter Diameter No. of

Catalog Number Length A B C Flutes

STEM-0950-025-06 90.4 9.6 6.1 4.6 4

STEM-0950-025-08 90.4 11.6 8.1 6.7 4

STEM-0950-025-10 90.4 13.4 9.9 8.5 4

STEM-0950-025-12 90.4 15.4 11.9 10.6 4

STEM-0950-025-14 90.4 17.5 14.0 12.6 4

Press-fit Stem Diameter Diameter Diameter Spline No. of

Catalog Number Length A B C Depth Splines

STEM-0920-025-06 90.4 11.6 6.8 4.6 1 12

STEM-0920-025-07 90.4 12.4 7.6 5.3 1 12

STEM-0920-025-08 90.4 13.7 9.0 6.6 1 12

STEM-0920-025-09 90.4 14.4 9.9 7.4 1 12

STEM-0920-025-10 90.4 15.4 10.9 8.5 1 12

STEM-0920-025-11 90.4 16.5 12.1 9.5 1 12

STEM-0920-025-12 90.4 17.5 13.2 10.6 1 12

STEM-0920-025-13 90.4 18.5 14.2 11.6 1 12

STEM-0920-025-14 90.4 19.5 15.3 12.6 1 12

STEM-0920-025-15 90.4 20.5 16.4 13.5 1 12

STEM-0920-025-16 90.4 21.5 17.4 14.7 1 12

Primary Body Max Max Base Trunnion

Catalog Number Height Length Width Diameter Offset

BOD-0923-020-08STD 35 16.9 11.6 11.6 8

BOD-0923-020-10SML 30 17.8 13.7 13.7 8

BOD-0923-020-10STD 35 18.1 13.7 13.7 8

BOD-0923-020-10LRG 40 18.3 13.7 13.7 8

BOD-0923-020-12STD 35 19.2 15.4 15.4 8

BOD-0923-020-14SML 30 20.4 17.5 17.5 8

BOD-0923-020-14STD 35 20.6 17.5 17.5 8

BOD-0923-020-14LRG 40 20.7 17.5 17.5 8

BSW-0920-021-01 Body Screw

Ordering Information and Implant Dimensions (continued)

Spherical Diameter Ø

Height

Width

Pegged and Keeled Glenoid Dimensions (mm), UHMWPE

Fin-Lock™ Glenoid Dimensions (mm), HXLPE

Keeled Glenoid Keel Keel Keel

Catalog Number Size H W Ø L H W

GLN-0920-030-00K X-Small 31.8 22.9 54 14.0 22.9 4.1

GLN-0920-030-01K Small 34.3 24.9 59 14.0 22.9 4.1

GLN-0920-030-02K Medium 36.8 26.9 64 15.2 25.4 5.1

GLN-0920-030-03K Large 39.4 28.9 66 15.2 25.4 5.1

Pegged Glenoid Peg L Peg L Peg

Catalog Number Size H W Ø Center Peripheral D

GLN-0920-030-00P X-Small 31.8 22.9 54 14.0 6.4 5.0

GLN-0920-030-01P Small 34.3 24.9 59 14.0 6.4 5.0

GLN-0920-030-02P Medium 36.8 26.9 64 15.2 6.4 5.0

GLN-0920-030-03P Large 39.4 28.9 66 15.2 6.4 5.0

Fin-Lock Glenoid Peg D Peg L Peg Outer Peg Inner Peg L

Catalog Number Size H W Ø D D

GLN-0926-030-00A X-Small 31.8 22.9 54 5.0 6.4 9.5

GLN-0926-030-01A Small 34.3 24.9 59 5.0 6.4 9.5

GLN-0926-030-02A Medium 36.8 26.9 64 5.0 6.4 9.5

GLN-0926-030-03A Large 39.4 28.9 66 5.0 6.4 9.5

Peripheral Center

5.5

15.0

18.0

23 2345678910111213141516171819202122 1

115 1322 1124 917 7 521 19 214 1216 1023 820 618 4 3

DRAWN

CHK'D

APPV'D

MFG

Q.A

UNLESS OTHERWISE SPECIFIED:

DIMENSIONS ARE IN MILLIMETERS

SURFACE FINISH:

TOLERANCES:

LINEAR:

ANGULAR:

FINISH:

DEBURR AND

BREAK SHARP

EDGES

NAME

SIGNATURE

DATE

MATERIAL:

DO NOT SCALE DRAWING

REVISION

TITLE:

DWG NO.

SCALE:5:1

SHEET 1 OF 1

WEIGHT:

mod-04-0926-030

23 2345678910111213141516171819202122 1

115 1322 1124 917 7 521 19 214 1216 1023 820 618 4 3

DRAWN

CHK'D

APPV'D

MFG

Q.A

UNLESS OTHERWISE SPECIFIED:

DIMENSIONS ARE IN MILLIMETERS

SURFACE FINISH:

TOLERANCES:

LINEAR:

ANGULAR:

FINISH:

DEBURR AND

BREAK SHARP

EDGES

NAME

SIGNATURE

DATE

MATERIAL:

DO NOT SCALE DRAWING

REVISION

TITLE:

DWG NO.

SCALE:5:1

SHEET 1 OF 1

WEIGHT:

mod-04-0926-030

Integra®

Titan™ Modular Shoulder System

USA 800-654-2873

888-980-7742 fax

International +1 609-936-5400

+1 609-750-4259 fax

integralife.com/contact

International +33 (0)4 37 47 59 50

+33 (0)4 37 47 59 25 fax

Benelux +32 (0)2 257 4130

+32 (0)2 253 2466 fax

France +33 (0)4 37 47 59 10

+33 (0)4 37 47 59 29 fax

Switzerland +41 (0)22 721 23 00

+41 (0)22 721 23 99 fax

United Kingdom +44 (0)1 264 345 781

+44 (0)1 264 363 782 fax

integralife.eu/contact

United States, Canada, Asia, Pacific, Latin America

Europe, Middle-East, Africa

Integra LifeSciences Services (France)

Immeuble Séquoia 2, 97 allée Alexandre Borodine

Parc technologique de la Porte des Alpes

69800 Saint Priest

France

EC REP

Ascension Orthopedics, Inc.

8700 Cameron Road, Suite 100

Austin, Texas 78754

USA

Manufacturer:

Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region.

Always refer to the appropriate instructions for use for complete clinical instructions.

Non contractual document. The manufacturer reserves the right, without prior notice, to modify the products in order to improve their quality.

Warning: Applicable laws restrict these products to sale by or on the order of a physician.

For more information or to place an order, please contact:

Integra and the Integra logo are registered trademarks of Integra LifeSciences Corporation or its subsidiaries in the United States and/or other countries.

Printed in USA. 0M 0440637-5-EN LC04-0926-003 Rev B

0440637 5 EN Fin Lock Surgical Technique

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