CD HORIZON® Spinal System 8104522
by Medtronic Sofamor Danek, Inc.
CD HORIZON® Spinal System 8104522 is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K061579 on 11 Aug 2006 and listed in FDA GUDID since 15 Jul 2015 (UDI-DI 00613994154903), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00613994154903 | Date15 Jul 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK061579 | Date11 Aug 2006 | StatusActive |
Official records
- AccessGUDID record 00613994154903
- FDA 510(k) database K061579
Across registries
- FDA 510(k) K061579 decided 11 Aug 2006 Active
- FDA GUDID UDI-DI 00613994154903 listed 15 Jul 2015 Listed
Timeline
- Cleared FDA 510(k) K061579
- Listed FDA GUDID 00613994154903
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- CD HORIZON® Spinal System
- Generic name
- Bone-screw internal spinal fixation system connector
- Model / reference
- 8104522
- Primary DI / UDI-DI
- 00613994154903
- 510(k) Number
- FDA product code
- MNH, KWQ, NKB, NQP, MNI, KWP
- GMDN term
- Bone-screw internal spinal fixation system connector
- Device class
- Class II
- Regulation number
- 888.3070, 888.3060, 888.3050
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 22.0 Millimeter
Similar devices in this category
Other devices filed under Bone-screw internal spinal fixation system connector.