Annextm Adjacent Level System
510(k) K132403
Annextm Adjacent Level System is a Class II device made by Spine Wave, Inc., cleared under FDA 510(k) K132403 on 10 Jan 2014, 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 | NumberK132403 | Date10 Jan 2014 | StatusActive |
Official records
- FDA 510(k) database K132403
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- Withdrawn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