Australia TGA ARTG recordEVOLUTION® Revision CCK Nonporous CoCr Femoral Knee Components - Uncoated knee femur prosthesis
Australia TGA ARTG Registered Device · MicroPort Orthopedics Pty Ltd · MicroPort Orthopedics Inc · Class III · Started May 09, 2019
Good Name: MicroPort Orthopedics Pty Ltd - EVOLUTION® Revision CCK Nonporous CoCr Femoral Knee Components - Uncoated knee femur prosthesis
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- May 09, 2019
- Effective Date
- May 09, 2019
- Country
- United States of America
- Address
- 5677 Airline Road, Arlington, TN, 38002
A total knee system component used to replace the distal femur. Indicated for use in knee arthroplasty in skeletally mature patients with the following condition: 1) revision procedures where other treatments or devices have failed.
Access comprehensive regulatory information for EVOLUTION® Revision CCK Nonporous CoCr Femoral Knee Components - 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 MicroPort Orthopedics Pty Ltd, manufactured by MicroPort Orthopedics Inc in United States of America. The device registration started on May 09, 2019.
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.