Australia flagARTG 317407

EVOLUTION® Revision Tibial Base Non-Porous - Uncoated knee tibia prosthesis, metallic

ARTG ID: 317407 · MicroPort Orthopedics Pty Ltd · MicroPort Orthopedics Inc · Class III · Started May 09, 2019

Good Name: MicroPort Orthopedics Pty Ltd - EVOLUTION® Revision Tibial Base Non-Porous - Uncoated knee tibia prosthesis, metallic

Device classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
317407
Start Date
May 09, 2019
Effective Date
May 09, 2019
Sponsor
Manufacturer
Country
United States of America
Address
5677 Airline Road, Arlington, TN, 38002
Intended purpose

A total knee system component used to replace the proximal tibia. Indicated for use in knee arthroplasty in skeletally mature patients with the following condition: 1) revision procedures where other treatments or devices have failed.

About this record

Access comprehensive regulatory information for EVOLUTION® Revision Tibial Base Non-Porous - Uncoated knee tibia prosthesis, metallic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 317407 and sponsored by MicroPort Orthopedics Pty Ltd, manufactured by MicroPort Orthopedics Inc in United States of America. The device registration started on May 09, 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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