STALIF FLX - Spinal cage - ARTG 482085
Access comprehensive regulatory information for STALIF FLX - Spinal cage in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 482085 and sponsored by Actis Medical Pty Ltd, manufactured by Centinel Spine LLC in United States of America. The device registration started on March 07, 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.
The STALIF FLX is intended for use as an intervertebral body fusion cage at one or two contiguous levels, typically to treat patients with symptomatic degenerative disc disease (DDD). The device is fixed to the superior and inferior vertebral bodies by cancellous fixation screws, and may be used with graft material (not provided with the device). The device is manufactured from titanium alloy, and provided sterile.