Main information

  • Trade name:
  • Reclaim Distal Tapered Stem - Press-fit hip femur prosthesis, modular
  • Class:
  • Class III
  • Medicine domain:
  • Humans
  • Medicine type:
  • Medical device



  • Available in:
  • Reclaim Distal Tapered Stem - Press-fit hip femur prosthesis, modular
  • Language:
  • English

Other information


  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 219278
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:


Johnson & Johnson Medical Pty Ltd T/A Depuy Australia - Reclaim Distal Tapered Stem - Press-fit hip

femur prosthesis, modular

ARTG entry for

Medical Device Included Class III


Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes

Postal Address

PO Box 134,NORTH RYDE, NSW, 2113


ARTG Start Date


Product category

Medical Device Class III



Approval area

Medical Devices


- 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.




Depuy (Ireland)

Loughbeg Ringaskiddy




1. Reclaim Distal Tapered Stem - Press-fit hip femur prosthesis, modular

Product Type

Single Device Product

Effective date



55833 Press-fit hip femur prosthesis, modular

Functional description

The Reclaim Distal Tapered Stem is made from titanium and allows for the press-fit of the Reclaim

Proximal Body. The Reclaim Distal Tapered Stem is grit-blasted allowing for cementless fixation into the

femoral canal.

Intended purpose

The Reclaim Tapered Distal Stem is the femoral stem component of the Reclaim revision hip system and

is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint

articulation in patients where there is evidence of sufficient sound bone to seat and support the

components. The RECLAIM Revision Hip System is indicated for cementless use in the treatment of failed

previous hip surgery, including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface

replacement arthroplasty, or other total hip replacement

Variant information

Length (mm) 140 - 290

Offset Straight or 3 deg

Diameter (mm) 14-31

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

Public Summary

Page 1 of

Produced at 02.12.2017 at 04:39:22 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 for contact information