Spine Implant
- UID
- IMP/MD/2018/000224_7f7e6aefdb08e44a88c70decf2b1de8d_bbc6f243bcb3f5e015c25090ea98c03d
- 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 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000224_7f7e6aefdb08e44a88c70decf2b1de8d_bbc6f243bcb3f5e015c25090ea98c03d. 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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