Summary for ARTG Entry:
Zimmer Biomet Pty LtdPty Ltd - AGC V2 Total Knee Anatomic Porous Posterior Stabilised Femoral
Component - Posterior-stabilized total knee 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.
Biomet UK Ltd
Waterton Industrial Estate
Bridgend, South Glamorgan, CF31 3XA
1. AGC V2 Total Knee Anatomic Porous Posterior Stabilised Femoral Component - Posterior-stabilized total
Single Device Product
33665 Posterior-stabilized total knee prosthesis
Titanium porous coated chrome cobalt cruciate substituting femoral knee component with deep patella
track, wide femoral condyles
Porous coated chrome cobalt femoral component for cementless use in AGC V2 Total Knee arthroplasty
when the cruciate ligament requires substitution; to provide a means of reducing pain and restoring
function. The indications for use include: Osteoarthritis, rheumatoid arthritis; Traumatic arthritis; Failure of
a previous joint replacement procedure; Correction of varus, valgus or post-traumatic deformity; Correction
or revision of unsuccessful osteotomy or arthrodesis.
Size (mm) 55 to 80
No Specific Conditions included on Record
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Produced at 10.11.2017 at 12:48:22 AEDT
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