ARTG 421975Spinal cage
ARTG ID: 421975 · Precision Surgical Pty Ltd · SpineVision SAS · Class IIb · Started September 18, 2023
Good Name: Precision Surgical Pty Ltd - Spinal cage
- Risk Class
- Class IIb
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 421975
- Start Date
- September 18, 2023
- Effective Date
- September 18, 2023
- Name
- SpineVision SAS
- Country
- France
- Address
- Batiment E 10 Rue de la Renaissance, Antony, 92160
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.
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.