Bio-Modular

Main information

  • Trade name:
  • Bio-Modular Pegged Glenoid - Prosthesis, internal, joint, shoulder, glenoid component
  • Class:
  • Class III
  • Medicine domain:
  • Humans
  • Medicine type:
  • Medical device

Documents

Localization

  • Available in:
  • Bio-Modular Pegged Glenoid - Prosthesis, internal, joint, shoulder, glenoid component
    Australia
  • Language:
  • English

Other information

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 218752
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:

218752

Zimmer Biomet Pty Ltd - Bio-Modular Pegged Glenoid - Prosthesis, internal, joint, shoulder, glenoid

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

21/12/2013

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. Bio-Modular Pegged Glenoid - Prosthesis, internal, joint, shoulder, glenoid component

Product Type

Single Device Product

Effective date

21/12/2013

GMDN

36259 Prosthesis, internal, joint, shoulder, glenoid component

Functional description

Glenoid base component shoulder joint replacement prostheses with x-ray marker. Made from

UHMWPE/Tantalum

Intended purpose

The Pegged Glenoid is part of the Bio-Modular Shoulder System and is intended for partial or total

shoulder joint arthroplasty.

Variant information

Size medium

Size large

Size small

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 09:26:50 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

14-11-2018

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FDA - U.S. Food and Drug Administration

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28-8-2018

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28-8-2018

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22-8-2018

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20-8-2018

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