Vanguard

Main information

  • Trade name:
  • Vanguard Knee Cruciate Retaining Porous femoral component - Coated knee femur prosthesis
  • Class:
  • Class III
  • Medicine domain:
  • Humans
  • Medicine type:
  • Medical device

Documents

Localization

  • Available in:
  • Vanguard Knee Cruciate Retaining Porous femoral component - Coated knee femur prosthesis
    Australia
  • Language:
  • English

Other information

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 218495
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:

218495

Zimmer Pty Ltd - Vanguard Knee Cruciate Retaining Porous femoral component - Coated knee femur

prosthesis

ARTG entry for

Medical Device Included Class III

Sponsor

Zimmer Biomet Pty Ltd

Postal Address

Locked Bag 1310,FRENCHS FOREST, NSW, 2086

Australia

ARTG Start Date

13/12/2013

Product category

Medical Device Class III

Status

Active

Approval area

Medical Devices

Conditions

- The inclusion of the kind of device in the ARTG is subject to compliance with all conditions placed or imposed on the ARTG entry. Refer Part 4-5,

Division 2 (Conditions) of the Therapeutic Goods Act 1989 and Part 5, Division 5.2 (Conditions) of the Therapeutic Goods (Medical Devices) Regulations

2002 for relevant information.

- Breaching conditions of the inclusion related to the device of the kind may lead to suspension or cancellation of the ARTG entry; may be a criminal

offence; and civil penalties may apply.

Manufacturers

Name

Address

Biomet Orthopedics

56 East Bell Drive

Warsaw, IN, 46581

United States Of America

Products

1. Vanguard Knee Cruciate Retaining Porous femoral component - Coated knee femur prosthesis

Product Type

Single Device Product

Effective date

13/12/2013

GMDN

33745 Coated knee femur prosthesis

Functional description

Cruciate retaining porous coated femoral component for use in total knee arthroplasty. The CR femoral

component has removable lugs to allow for posterior and distal augment options. This component must be

used with a tibial tray component and one of 3 cruciate retaining bearing options.

Intended purpose

Chrome/cobalt/molybdenum alloy cruciate retaining femoral component for use in knee joint replacement

due to

1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis

where one or more compartments are involved

2) correction of varus, valgus, or posttraumatic deformity

3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement

procedure

The porous coated device is intended for uncemented use.

Variant information

Size (mm) 55-80

Product name (see guidance docs) Left

Product name (see guidance docs) Right

Specific Conditions

No Specific Conditions included on Record

© Commonwealth of Australia.This work is copyright.You are not permitted to re-transmit, distribute or commercialise the material without obtaining prior

written approval from the Commonwealth.Further details can be found at http://www.tga.gov.au/about/website-copyright.htm.

Public Summary

Page 1 of

Produced at 10.11.2017 at 10:15:57 AEDT

This is not an ARTG Certificate document.

The onus is on the reader to verify the current accuracy of the information on the document subsequent to the date shown.

Visit www.tga.gov.au for contact information