Australia TGA ARTG recordTiNbN Coated Vanguard Complete Knee Posterior Stabilised Interlok Femoral Component - Uncoated knee femur prosthesis
Australia TGA ARTG Registered Device · Zimmer Biomet Pty Ltd · Biomet UK Ltd · Class III · Started September 07, 2017
Good Name: Zimmer Biomet Pty Ltd - TiNbN Coated Vanguard Complete Knee Posterior Stabilised Interlok Femoral Component - Uncoated knee femur prosthesis
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- September 07, 2017
- Effective Date
- September 07, 2017
- Name
- Biomet UK Ltd
- Country
- United Kingdom
- Address
- Waterton Industrial Estate, Bridgend, South Glamorgan, CF31 3XA
Chrome/cobalt/molybdenum alloy posterior stabilised femoral component, with titanium niobium nitride coating, for use in knee joint replacement due to Osteoarthritis, rheumatoid arthritis or 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. Intended for cemented use in nickel sensitive patients.
Access comprehensive regulatory information for TiNbN Coated Vanguard Complete Knee Posterior Stabilised Interlok Femoral Component - Uncoated knee femur prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Zimmer Biomet Pty Ltd, manufactured by Biomet UK Ltd in United Kingdom. The device registration started on September 07, 2017.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.