K261363
- 510(k) number
- K261363
- Device name
- Y-Knotless Flex Anchors
- Applicant
- CONMED Corporation NY · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2026-05-13
- Date received
- 2026-04-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K261363.pdf
Official FDA record: K261363
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.