Vanguard® 360 Revision Knee System

Zimmer Biomet’s Vanguard 360 Revision Knee System allows the surgeon to provide an appropriate solution for each individual patient. The independent sizing of femoral and tibial components, along with the capability to position the universal femoral and tibial stem offsets in a full 360 degree range allow for complete intraoperative flexibility. This flexibility provides options to effectively address bone loss, which works to deliver personalized patient care. The Vanguard 360 Revision Knee incorporates the tibial design and key Vanguard Complete Knee Systems femoral component design features to deliver customizable implant combinations.     

 

Features of the Vanguard 360 Revision Knee System include:

  • Nine tibial sizes
  • Ten femoral sizes
  • Complete tibial/femoral interchangeability
  • A variety of stem options and offset adapters for precise component positioning
  • An offset stem adapter, universal to both femoral and tibial components, which rotates 360 degrees for precise positioning
  • Independent distal and posterior augments provide a solution to address bone loss
  • The same symmetrical shape from the Vanguard Complete Knee System
  • Clinically proven polyethylene bearing locking mechanism
  • Comprehensive, precise, intuitive instrumentation

 

The Vanguard 360 Revision Knee System offers a seamless transition from a Vanguard Primary Knee. The design features and instrumentation allow surgeons to achieve optimal component positioning and efficiently address unique patient anatomies.

Product Features

The Zimmer Biomet Vanguard 360 Revision Knee System consists of customizable implant combinations. The independent fit of each component and comprehensive instrumentation aid surgeons in addressing diverse, often challenging procedures. At the same time, the customizable components allow surgeons to deliver a personalized patient approach to revision knee surgery. The benefits of the Vanguard 360 Revision Knee System include:

  • Complete tibial-femoral interchangeability with multiple offsets and stem options
  • A precise, intuitive instrumentation platform, featuring simplified trial first approach
  • Industry-leading level of constraint from the Vanguard SSK Revision Knee System
  • Smooth, grit-blasted, and splined stems in four lengths and a wide range of diameters for component fixation
  • Vanguard 360 PS Bearing: deeper anterior cutout, 15 degrees internal/external rotation, no varus/valgus constraint
  • Designed to provide the most constrained, non-hinged bearing in the industry for optimal stability in patients with ligament deficiencies1-4
  • Deep anterior relief to accommodate the patella tendon during high flexion
  • Modular small and large cruciate wing augments for extra rotational stability

Technology

ArCom® Polyethylene is clinically proven to be resistant to wear, delamination and oxidation1

Previous page

References

  1. Zimmer. Nexgen® Legacy® Constrained Condylar Knee (LCCK). http://zimmer.com/en-US/hcp/knee/product/nexgen-lcck.jspx
  2. DePuy Orthopaedics, Inc. Knee Revision ReferenceCards. 2M0807.
  3. Smith & Nephew. System Specification Guide and Product Catalog. 71281438, REVA, 11/10.
  4. Stryker. Overview of Triathlon® TS-Section ll-A: 36.Orthopaedics Learning System.

 

Legal Manufacturer:                      

Biomet Orthopedics
56 East Bell Drive 
P.O. Box 587
Warsaw, Indiana 46581 USA

All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet.  
This material is intended for health care professionals. Distribution to any other recipient is prohibited.
For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert and information on this website. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support.