# Mg OSTEOREVIVE™;Mg OSTEOCRETE™ (K262230): 510(k) cleared for Bone Solutions, Inc.

**Predicate Speed & CAPA Advisory Opportunity Score:** 30/100

| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K262230 |
| Device | Mg OSTEOREVIVE™;Mg OSTEOCRETE™ |
| Applicant | Bone Solutions, Inc. |
| Specialty / panel | Orthopedic |
| Product code | MQV |
| Device class | 2 |
| Clearance type | Traditional |
| Decision | Substantially Equivalent |
| Received | 2026-06-30 |
| Decision date | 2026-09-11 |
| Review time (days) | 73 |
| Third-party review | No |
| Applicant location | Colleyville, TX, US |

## Why this score
- Fast 73-day review: this device is a strong predicate for similar products.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K262230). Last refreshed: 2026-11-04T09:16:12.111Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.