Nuvasive Spherx System
510(k) K060225
Nuvasive Spherx System is a Class II device made by Nuvasive, Inc., cleared under FDA 510(k) K060225 on 12 Apr 2006, 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 | NumberK060225 | Date12 Apr 2006 | StatusActive |
Official records
- FDA 510(k) database K060225
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MNH
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3070
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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