Australia TGA ARTG recordSpinal cage
Australia TGA ARTG Registered Device · Stryker Australia Pty Ltd · Stryker Spine · Class IIb · Started March 17, 2021
Good Name: Stryker Australia Pty Ltd - Spinal cage
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 17, 2021
- Effective Date
- March 17, 2021
- Name
- Stryker Spine
- Country
- United States of America
- Address
- 2 Pearl Court, Allendale, NJ, 07401
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.
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 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.