Australia flagARTG 475839

PRODISC C VIVO - Cervical total disc replacement prosthesis

ARTG ID: 475839 · Centinel Spine Australia Pty Ltd · Centinel Spine LLC · Class III · Started January 15, 2025

Good Name: Centinel Spine Australia Pty Ltd - PRODISC C VIVO - Cervical total disc replacement prosthesis

Device classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
475839
Start Date
January 15, 2025
Effective Date
January 15, 2025
Sponsor
Manufacturer
Country
United States of America
Address
900 Airport Road Suite 3B, West Chester, PA, 19380
Intended purpose

Prostheses used to replace a cervical inter-vertebral disc and to restore disc height and segmental motion.

About this record

Access comprehensive regulatory information for PRODISC C VIVO - Cervical total disc replacement prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 475839 and sponsored by Centinel Spine Australia Pty Ltd, manufactured by Centinel Spine LLC in United States of America. The device registration started on January 15, 2025.

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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