Summary for ARTG Entry:
Zimmer Pty Ltd - NexGen® Complete Knee Solution Legacy® Knee LPS Femoral Component, Porous -
Coated knee femur prosthesis
ARTG entry for
Medical Device Included Class III
Zimmer Biomet Pty Ltd
Locked Bag 1310,FRENCHS FOREST, NSW, 2086
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.
1800 West Center Street
WARSAW, INDIANA, 46580
United States Of America
1. NexGen® Complete Knee Solution Legacy® Knee LPS Femoral Component, Porous - Coated knee femur
Single Device Product
33745 Coated knee femur prosthesis
The NexGen Legacy ®Knee LPS Femoral Component is a porous, semi-constrained, non-linked condylar
knee prosthesis made from Zimaloy Cobalt-Chromium-Molybdenum alloy intended for patients who, in the
surgeon's judgement, have adequate bone stock and varus/valgus stability, and/or when the surgeon
elects to substitute for the posterior cruciate ligament. Fixation method is porous fibre metal, cemented or
uncemented (biological fixation).
Femoral component of the NexGen® Complete Knee Solution Legacy® total knee arthroplasty system
indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis,
traumatic arthritis, polyarthritis. Collagen disorders, and/or avascular necrosis of the femoral condyle.
Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or
prior patellectomy. Moderate valgus, varus, or flexion deformities. The salvage of previously failed surgical
attempts or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery.
Porous coated LPS femoral components are intended for cemented or uncemented use in knee
No Specific Conditions included on Record
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