K251530
- 510(k) number
- K251530
- Device name
- CONMED Argo Knotless® Anchor
- Applicant
- Conmed Corporation NY · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2025-06-18
- Date received
- 2025-05-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251530.pdf
Official FDA record: K251530
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.