Zimmer

Main information

  • Trade name:
  • Zimmer® Unicompartmental Knee System, Articular Surface - Prosthesis, knee, internal, insert component
  • Class:
  • Class III
  • Medicine domain:
  • Humans
  • Medicine type:
  • Medical device

Documents

Localization

  • Available in:
  • Zimmer® Unicompartmental Knee System, Articular Surface - Prosthesis, knee, internal, insert component
    Australia
  • Language:
  • English

Other information

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 220168
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:

220168

Zimmer Pty Ltd - Zimmer® Unicompartmental Knee System, Articular Surface - Prosthesis, knee, internal,

insert component

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

14/02/2014

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

Zimmer Inc

1800 West Center Street

WARSAW, INDIANA, 46580

United States Of America

Products

1. Zimmer® Unicompartmental Knee System, Articular Surface - Prosthesis, knee, internal, insert component

Product Type

Single Device Product

Effective date

14/02/2014

GMDN

46585 Prosthesis, knee, internal, insert component

Functional description

Designed for the surface reconstruction of individual femoral/tibial condyles of a knee joint prosthesis when

load bearing ROM is expected to be less than or equal to 155 degrees. It is indicated for cemented use

only and is made from Ultra-High Molecular Weight polyethylene.

Intended purpose

Articular surface component of the Zimmer® Unicompartmental Knee System prosthesis indicated for

patients with:

- Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis.

- Previous tibial condyle or plateau fractures with loss of anatomy or function.

- Varus or valgus deformities.

- Revision of previous arthroplasty procedures.

Variant information

Size 1-6

Height (mm) 8-14

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 05:03:11 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