CD Horizon™ ModuLeX™ Spinal System 55946204530
by Medtronic Sofamor Danek, Inc. 2 variants
CD Horizon™ ModuLeX™ Spinal System 55946204530 is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K221244 on 25 May 2022 and listed in FDA GUDID since 31 Mar 2025 (UDI-DI 20763000972985), 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 | Number20763000972985 | Date31 Mar 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK221244 | Date25 May 2022 | StatusActive |
Official records
- AccessGUDID record 20763000972985
- FDA 510(k) database K221244
Across registries
- FDA 510(k) K221244 decided 25 May 2022 Active
- FDA GUDID UDI-DI 20763000972985 listed 31 Mar 2025 Listed
Timeline
- Cleared FDA 510(k) K221244
- Listed FDA GUDID 20763000972985
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- CD Horizon™ ModuLeX™ Spinal System
- Generic name
- Spinal bone screw, non-bioabsorbable
- Model / reference
- 55946204530
- Primary DI / UDI-DI
- 20763000972985
- 510(k) Number
- FDA product code
- NKB, KWQ, KWP
- GMDN term
- Spinal bone screw, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3070, 888.3060, 888.3050
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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