Bone-screw internal spinal fixation system, non-sterile - ARTG 330363
Access comprehensive regulatory information for Bone-screw internal spinal fixation system, non-sterile in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 330363 and sponsored by Equinox Medical Pty Ltd, manufactured by Shandong Weigao Orthopaedic Device Company Limited. in China. The device registration started on February 25, 2020.
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 device is indicated for spinal fixation including: 1) Degenerative diseases (eg, disc herniation, spinal stenosis, spondylolisthesis, lumbar instability); 2) Spinal deformities (eg, scoliosis, humpback and / or lordosis); 3) trauma (eg, fracture, and / or dislocation); 4) pseudarthrosis, tumor resection, and / or previous fusion fails.