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Femoral stem trial prosthesis

Access comprehensive regulatory information for Femoral stem trial prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Stryker Australia Pty Ltd, manufactured by Howmedica Osteonics Corporation in United States of America. The device registration started on February 15, 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 IIa
Class IIa
Femoral stem trial prosthesis
Australia TGA ARTG Registered Device
Good Name: Stryker Australia Pty Ltd - Femoral stem trial prosthesis
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Intended Purpose

Invasive manual surgical instruments intended for use during hip, knee and osteosynthesis orthopaedic surgeries.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 15, 2023
Effective Date
February 15, 2023
Manufacturer
Country
United States of America
Address
325 Corporate Drive, Mahwah, New Jersey, 07430