AONA Implant Instrument and Technique Guide Series

 Titanium Distal Femoral Nail System ®
For Retrograde Insertion

Technique Guide

Titanium Distal Femoral Nail - Retrograde Insertion  Titanium Femoral Distal Nail - Retrograde Insertion Titanium Distal Femoral Nail - Retrograde Insertion   Titanium Distal Femoral Nail - Retrograde Insertion  
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Table of Contents

Indications

Preoperative Implant Selection

Technique

  • Opening the Distal Femur
  • Instruments to Insert the Nail
  • Inserting the Nail
  • Instruments to Lock Distally
  • Locking Distally
  • Locking Proximally
  • Inserting the End Cap
  • Implant Removal

    Product Information

  • Implant Specifications
  • Set Contents
    Next Page

    AONA Technique Guide Index

    The material presented by AO North America on this website is directed to orthopaedic surgeons, neurosurgeons, plastic and maxillofacial surgeons, and veterinary surgeons in North America, and is intended for educational and communication purposes only. Any clinical matters which may be discussed either in videos or individual case presentations, represent the opinions or approach of the individual physicians presenting the material. AONA exerts no editorial control over the contents.

    AONA represents that there are a variety of approaches to treating a particular medical condition. The material discussed is not intended to represent the only or necessarily the best method or procedure, but conveys the opinion of the individual author. AONA assumes no responsibility for the individual decision to use any device or technique to treat a specific medical problem. The decision to use a particular technique rests solely between the patient and the treating surgeon. It is recommended that, prior to using a demonstrated technique, a surgeon participate in an AONA sponsored educational course.

    Some medical devices demonstrated in the material have FDA clearance for specific indications; some are available only in restricted settings. It is the responsibility of the treating surgeon to determine the FDA status of the device to be used, and to use the product(s) with the appropriate patient consent and in compliance with applicable law.

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