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Spinal cage

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 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.

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TGA ARTG Official Data
Class IIb
Class IIb
Spinal cage
Australia TGA ARTG Registered Device
Good Name: Precision Surgical Pty Ltd - Spinal cage
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Intended Purpose

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.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
September 18, 2023
Effective Date
September 18, 2023
Manufacturer
Country
France
Address
Batiment E 10 Rue de la Renaissance, Antony, 92160