Phoenix Antegrade Surgical Technique
2016-04-01
: Pdf Phoenix Antegrade Surgical Technique Phoenix_Antegrade_Surgical_Technique 4 2016 pdf
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Phoenix ™ Antegrade Femoral Nail System Featuring CoreLock ™ Technology • Each trochanteric and piriformis fossa entry point nail features patent pending CoreLock ™ Technology, a preassembled, screw retention mechanism • In the reconstructive mode, CoreLock ™ will limit the sliding of two 6.0mm cannulated reconstructive screws and in the interlock mode, will allow a single 5.0mm fully threaded screw to be mechanically locked to the nail Phoenix ™ Antegrade Femoral Nail System Featuring CoreLock ™ Technology • The Phoenix ™ Antegrade Femoral Nail System consists of trochanteric and piriformis fossa entry point nails that allow for either reconstructive or interlock screw applications • Each nail features patent pending CoreLock ™ Technology, a preassembled, screw retention mechanism. In the reconstructive mode, CoreLock ™ Technology will limit the sliding of two 6.0mm cannulated reconstructive screws. Alternatively, the CoreLock ™ Technology used in the interlock mode will allow a single 5.0mm fully threaded screw to be mechanically locked to the nail. • Nails are available in diameters of 9.0mm, 10.5mm, 12.0mm, 13.5mm and 15.0mm varying in lengths ranging from 280mm-480mm (20mm increments) Piriformis Fossa Nail With Proximal Interlock Screw • Both Antegrade Femoral Nails are colored coded for left and right applications, facilitating intraoperative efficiencies Trochanteric Nail With Reconstructive Screws Trochanteric Nail Specifications 55° 32mm 25mm 85mm 128° Neck Angle 11.5mm 17.5mm 6° bend • Each Antegrade Femoral nail is composed of titanium alloy and incorporates a 1.8m radius of curvature, 9° of built-in anteversion, a 128° femoral neck angle and allows for static or dynamic distal locking • Modular Radiolucent Targeting Arm permits multiplanar radiographic visualization that allows for accurate reconstructive or interlock targeting All trademarks herein are the property of Biomet, Inc. or its subsidiaries unless otherwise indicated. This material is intended for the sole use and benefit of the Biomet sales force and health care professionals. It is not to be redistributed, duplicated or disclosed without the express written consent of Biomet. For product information, including indications, contraindications, warnings, precautions and potential adverse effects, see the package insert and Biomet’s website. Responsible Manufacturer Biomet, Inc. P.O. Box 587 56 E. Bell Drive Warsaw, Indiana 46581-0587 USA ©2013 Biomet Orthopedics • Form No. BMET0309.0 • REV013013 www.biomet.com Rx only.
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