NuVasive AttraX Scaffold
510(k) K240507
NuVasive AttraX Scaffold is a Class II device made by Nuvasive, Inc., cleared under FDA 510(k) K240507 on 20 Mar 2024, 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 | NumberK240507 | Date20 Mar 2024 | StatusActive |
Official records
- FDA 510(k) database K240507
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQV
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3045
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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