Mg OSTEOREVIVE™
510(k) K262230
Mg OSTEOREVIVE™ is a Class II device made by Bone Solutions, Inc., cleared under FDA 510(k) K262230 on 11 Sep 2026, active as of 25 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 | NumberK262230 | Date11 Sep 2026 | StatusActive |
Official records
- FDA 510(k) database K262230
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- Withdrawn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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