NexGen

Main information

  • Trade name:
  • NexGen® Complete Knee Solution Legacy® Knee Posterior Stabilised PROLONG™ Highly Crosslinked Polyethylene LPS-Flex Art Surface -
  • Class:
  • Class III
  • Medicine domain:
  • Humans
  • Medicine type:
  • Medical device

Documents

Localization

  • Available in:
  • NexGen® Complete Knee Solution Legacy® Knee Posterior Stabilised PROLONG™ Highly Crosslinked Polyethylene LPS-Flex Art Surface -
    Australia
  • Language:
  • English

Other information

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 222148
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:

222148

Zimmer Pty Ltd - NexGen® Complete Knee Solution Legacy® Knee Posterior Stabilised PROLONG™

Highly Crosslinked Polyethylene LPS-Flex Art 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

8/04/2014

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. NexGen® Complete Knee Solution Legacy® Knee Posterior Stabilised PROLONG™ Highly Crosslinked

Polyethylene LPS-Flex Art Surface - Prosthesis, inter - Prosthesis, knee, internal, insert component

Product Type

Single Device Product

Effective date

8/04/2014

GMDN

46585 Prosthesis, knee, internal, insert component

Functional description

The articulating surface has a spine which interacts with the femoral cam. The LPS-Flex articulating

surface has a deeper anterior patellar cut-out to provide clearance for the patella bone and patella tendon

in high flexion. The articulating surface is made of PROLONG™ highly cross-linked UHMWPE and it has a

dovetail locking mechanism that is snapped into place on the tibial baseplate. For use with plate 1,2; 3,4;

5,6; 7,8,9,10. Compatible with LCCK Femoral components.

Intended purpose

Indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis,

traumatic arthritis, polyarthritis. Collagen disorders, and/or avascular necrosis of the femoral condyle.

Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or

prior patellectomy. Moderate valgus, varus, or flexion deformities. The salvage of previously failed surgical

attempts or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery.

Variant information

Height (mm) 10-14

Size GH

Size CD

Size AB

Size EF

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 09.11.2017 at 10:37:21 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