Artificial Cervical Disc
- UID
- IMP/MD/2019/000037_bd3b00880946f4bd4c670cd2df42de50_e0eff8cb297d9f8b651ae9c93f54a34d
- Device class
- Class C
- Brand name
- CD HORIZON SOLERA Spinal System
- License holder
- India Medtronic Private Limited
- Approving authority
- CDSCO
- Product information
- The PRESTIGE® Cervical Disc is generally indicated for use at any level from C2/C3 to C7/T1: - for cervical degenerative discopathy and instability • in patients with adjacent levels either congenitally or surgically fused • for primary surgery for degenerative discopathies or extensive anterior decompression • revision surgery for failed disc operation, stenosis, post-operative instability - pseudarthrosis or failed arthrodesis
Artificial Cervical Disc is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000037_bd3b00880946f4bd4c670cd2df42de50_e0eff8cb297d9f8b651ae9c93f54a34d. This device is marketed under the brand name CD HORIZON SOLERA Spinal System. The license holder is India Medtronic Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.
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