K260561
- 510(k) number
- K260561
- Device name
- Arthrex FiberTak Suture Anchor
- Applicant
- Arthrex, Inc. FL · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2026-03-20
- Date received
- 2026-02-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K260561.pdf
Official FDA record: K260561
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.