K240194
- 510(k) number
- K240194
- Device name
- ProCinch, QuadCinch
- Applicant
- Riverpoint Medical OR · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2024-02-21
- Date received
- 2024-01-24
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K240194.pdf
Official FDA record: K240194
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.