K242372
- 510(k) number
- K242372
- Device name
- Mg OSTEOREVIVE, Mg OSTEOCRETE
- Applicant
- Bone Solutions, Inc. TX · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-10-18
- Date received
- 2024-08-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242372.pdf
Official FDA record: K242372
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.