K253524
- 510(k) number
- K253524
- Device name
- Adaptos®Fuse Bone Graft
- Applicant
- Biomendex OY FI
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2026-02-17
- Date received
- 2025-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K253524.pdf
Official FDA record: K253524
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.