K251522
- 510(k) number
- K251522
- Device name
- Mg OSTEOINJECT; Mg OSTEOREVIVE; Mg OSTEOCRETE
- Applicant
- Bone Solutions, Inc. TX · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2025-10-13
- Date received
- 2025-05-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K251522.pdf
Official FDA record: K251522
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.