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Bone-screw internal spinal fixation system, non-sterile

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 I is 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 March 12, 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.

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TGA ARTG Official Data
Class I
Class I
Bone-screw internal spinal fixation system, non-sterile
Australia TGA ARTG Registered Device
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Bone-screw internal spinal fixation system, non-sterile
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Intended Purpose

Non-sterile devices associated with an assembly of devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
March 12, 2019
Effective Date
March 12, 2019
Manufacturer
Country
United States of America
Address
325 Paramount Drive, Raynham, Massachusetts, 02767