K240090
- 510(k) number
- K240090
- Device name
- Argo Knotless GENESYS Anchor
- Applicant
- Conmed Corporation NY · US
- Product code
- MAI — Fastener, Fixation, Biodegradable, Soft Tissue
- Decision date
- 2024-03-05
- Date received
- 2024-01-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K240090.pdf
Official FDA record: K240090
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.