Summary for ARTG Entry:
Stryker Australia Pty Ltd - AVON PATELLA COMPONENT - Polyethylene patella prosthesis
ARTG entry for
Medical Device Included Class III
Stryker Australia Pty Ltd
PO Box 970,ARTARMON, NSW, 1570
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.
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah, New Jersey, 07430
United States Of America
1. AVON PATELLA COMPONENT - Polyethylene patella prosthesis
Single Device Product
34199 Polyethylene patella prosthesis
A sterile implantable patella component of the AVON Patello-Femoral Joint Replacement system made of
polyethylene (UHMWPE), and designed to articulate with an artificial femoral component. For cemented
Intended to replace the patella during reconstruction of the patellofemoral joint. Patello-femoral Joint
Prostheses are intended to be used in cemented patellofemoral arthroplasty in patients with degenerative
arthritis in the distal femur and patella, patients with a history of patellar dislocation or patella fracture, or
patients with failed previous surgery (arthroscopy, tibial tubercle elevation, lateral release) where pain,
deformity or dysfunction persists.
Thickness 9.0mm - 10.0mm
Width (mm) M/L 35.9mm - 43.9mm
Height (mm) A/P 28.6mm - 34.8mm
No Specific Conditions included on Record
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