Spinal cage - ARTG 356926
Access comprehensive regulatory information for Spinal cage in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 356926 and sponsored by Stryker Australia Pty Ltd, manufactured by Stryker Spine in United States of America. The device registration started on March 17, 2021.
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.
An interbody fusion device indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as an adjunct to fusion in patients with Degenerative Disc Disease (DDD) at one or two contiguous levels from L2-S1.