Leva Spacer System
by Spine Wave, Inc. 2 variants
510(k) K151581
Leva Spacer System is a Class II device made by Spine Wave, Inc., cleared under FDA 510(k) K151581 on 9 Jul 2015, 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 | NumberK151581 | Date9 Jul 2015 | StatusActive |
Official records
- FDA 510(k) database K151581
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MAX
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3080
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent