K251309
- 510(k) number
- K251309
- Device name
- OSSIOfiber® Suture Anchor
- Applicant
- OSSIO , Ltd. IL
- Product code
- MAI — Fastener, Fixation, Biodegradable, Soft Tissue
- Decision date
- 2025-05-27
- Date received
- 2025-04-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251309.pdf
Official FDA record: K251309
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.