Summary for ARTG Entry:
Johnson & Johnson Medical Pty Ltd T/A Depuy Australia - Attune Posterior Stabilised Cemented Femur -
Uncoated knee femur prosthesis
ARTG entry for
Medical Device Included Class III
Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes
PO Box 134,NORTH RYDE, NSW, 2113
ARTG Start Date
Medical Device Class III
- 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.
COUNTY CORK, ,
1. Attune Posterior Stabilised Cemented Femur - Uncoated knee femur prosthesis
Single Device Product
32831 Uncoated knee femur prosthesis
The Attune Posterior Stabilised Cemented Femur is made of cobalt chrome and its implantation is
performed with bone cement. The Attune Posterior Stabilised Cemented Femur articulates with an Attune
posterior stabilised tibial insert.
The Attune Posterior Stabilised Cemented Femur is the femoral component of the Attune Total Knee
replacement system and is intended to provide increased patient mobility and reduced pain by replacing
the damaged knee joint in patients where there is evidence of sufficient sound bone to seat and support
Shape Standard or Narrow
Shape Lef or Right
No Specific Conditions included on Record
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This is not an ARTG Certificate document.
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