Australia TGA ARTG record

Orthopaedic bone distractor

Australia TGA ARTG Registered Device · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Spine Inc · Class I · Started March 12, 2019

Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Orthopaedic bone distractor

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

Sponsor

Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes

Manufacturer

Name: Depuy Spine Inc
Country: United States of America
Address: 325 Paramount Drive, Raynham, Massachusetts, 02767

Intended purpose

A hand-held manual surgical instrument designed to distract two bone surfaces to enable a surgical procedure.

About this record

Access comprehensive regulatory information for Orthopaedic bone distractor 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.