ARTG 482085STALIF FLX - Spinal cage
ARTG ID: 482085 · Actis Medical Pty Ltd · Centinel Spine LLC · Class IIb · Started March 07, 2025
Good Name: Actis Medical Pty Ltd - STALIF FLX - Spinal cage
- Risk Class
- Class IIb
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 482085
- Start Date
- March 07, 2025
- Effective Date
- March 07, 2025
- Country
- United States of America
- Address
- 900 Airport Road Suite 3B, West Chester, PA, 19380
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.
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.