Verte-Span Spinal System
by Medtronic Sofamor Danek, Inc.
510(k) K024049
Verte-Span Spinal System is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K024049 on 26 Feb 2003, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK024049 | Date26 Feb 2003 | StatusActive |
Official records
- FDA 510(k) database K024049
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQP
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3060
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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