Spine Implant - Screw
- UID
- IMP/MD/2018/000224_442152ea5fbaf61f4598d9e03ba45f03_a6a35e032f0cc53443c665c6723c9792
- Device class
- Class C
- Brand name
- AVS Anchor-L Cage System
- License holder
- Stryker India Pvt. Ltd.,
- Approving authority
- CDSCO
- Product information
- The Xia Spinal System is intended for anterior/anterolateral and posterior, noncervical pedicle and non-pedicle fixation of the spine to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc disease (AVS Anchor-L Cage System) (AVS Anchor-L Cage System); spondylolisthesis, trauma (AVS Anchor-L Cage System), spinal stenosis, curvatures (AVS Anchor-L Cage System), tumor, pseudoarthrosis and failed previous fusion. The 6 mm diameter rods from the DIAPASONTM Spinal System and OPUSTM Spinal System are intended to be used with the other components of the XIAR Titanium Spinal System. The Titanium Multi-Axis Cross-Connectors are intended to be used with the other components of the XIAR Titanium Spinal System
Spine Implant - Screw is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000224_442152ea5fbaf61f4598d9e03ba45f03_a6a35e032f0cc53443c665c6723c9792. This device is marketed under the brand name AVS Anchor-L Cage System. The license holder is Stryker India Pvt. Ltd.,, and it is classified as Device Class Class C. The approving authority is CDSCO.
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