K251408
- 510(k) number
- K251408
- Device name
- OsteoSight Hip (v1)
- Applicant
- Naitive Technologies, Ltd. GB
- Product code
- SAO — Radiology Software For Opportunistic Evaluation Of L
- Decision date
- 2025-09-02
- Date received
- 2025-05-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251408.pdf
Official FDA record: K251408
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.