ARTG 316060Bone-screw internal spinal fixation system, non-sterile
ARTG ID: 316060 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Spine Inc · Class IIb · Started April 02, 2019
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Bone-screw internal spinal fixation system, non-sterile
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 316060
- Start Date
- April 02, 2019
- Effective Date
- April 02, 2019
- Name
- Depuy Spine Inc
- Country
- United States of America
- Address
- 325 Paramount Drive, Raynham, Massachusetts, 02767
An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.
Access comprehensive regulatory information for Bone-screw internal spinal fixation system, 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 316060 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 02, 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.