Turon to RSP Conversion Module - Reverse shoulder prosthesis - ARTG 302688
Access comprehensive regulatory information for Turon to RSP Conversion Module - Reverse shoulder prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 302688 and sponsored by Mathys Orthopaedics Pty Ltd, manufactured by Encore Medical LP in United States of America. The device registration started on May 07, 2018.
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.
The Reverse Humeral Socket Shell (Turon to RSP Conversion Shell) is indicated for revision surgeries in patients with a grossly rotator cuff deficient shoulder joint with severe arthropathy or a previously failed joint replacement with a grossly rotator cuff deficient shoulder joint. The patient’s joint must be anatomically and structurally suited to receive the selected implant(s), and a functional deltoid muscle is necessary to use the device. The socket shell is only indicated for use with a well fixed Turon Humeral Stem.