K241932
- 510(k) number
- K241932
- Device name
- OSSIOfiber® Compression Staple
- Applicant
- OSSIO , Ltd. IL
- Product code
- MNU — Staple, Absorbable
- Decision date
- 2024-08-28
- Date received
- 2024-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K241932.pdf
Official FDA record: K241932
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.