Summary for ARTG Entry:
Stryker Australia Pty Ltd - AVON FEMORAL COMPONENT - Uncoated knee femur 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 FEMORAL COMPONENT - Uncoated knee femur prosthesis
Single Device Product
32831 Uncoated knee femur prosthesis
A sterile implantable femoral component of the AVON Patello-Femoral Joint Replacement system made of
Cobalt Chrome (Vitallium) and designed to articulate with an artificial patella. For cemented use only.
Intended to replace the femoral articulating surface 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.
Length (mm) A/P 42.5mm - 49.0mm
Width (mm) M/L 43.5mm - 54.3mm
Size XS - L
No Specific Conditions included on Record
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