ARTG 315998Polymeric spinal fusion cage, non-sterile
ARTG ID: 315998 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Spine Inc · Class IIb · Started April 01, 2019
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Polymeric spinal fusion cage, non-sterile
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 315998
- Start Date
- April 01, 2019
- Effective Date
- April 01, 2019
- Name
- Depuy Spine Inc
- Country
- United States of America
- Address
- 325 Paramount Drive, Raynham, Massachusetts, 02767
A non-sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae.
Access comprehensive regulatory information for Polymeric spinal fusion cage, non-sterile in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 315998 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy Spine Inc in United States of America. The device registration started on April 01, 2019.
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.