K250216
- 510(k) number
- K250216
- Device name
- OsteoProbe (OP-100)
- Applicant
- Active Life Scientific, Inc. CA · US
- Product code
- QGQ — Bone Indentation Device
- Decision date
- 2025-09-11
- Date received
- 2025-01-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K250216.pdf
Official FDA record: K250216
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.