K233302
- 510(k) number
- K233302
- Device name
- OSSIOfiber® Compression Staple
- Applicant
- OSSIO , Ltd. IL
- Product code
- MNU — Staple, Absorbable
- Decision date
- 2023-11-16
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K233302.pdf
Official FDA record: K233302
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.