Spinal cage - ARTG 421975
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 421975 and sponsored by Precision Surgical Pty Ltd, manufactured by SpineVision SAS in France. The device registration started on September 18, 2023.
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 ACIF (Anterior Cervical Interbody Fusion) spinal fusion device is intended as a standalone intervertebral body fusion device of the spine. It is intended to be implanted via an anterior approach to give a primary stability of the spinal column (with or without restoring disc height) until fusion occurs.