K261707
- 510(k) number
- K261707
- Device name
- MEMO 4D Curve Semirigid mitral annuloplasty ring
- Applicant
- Corcym S.r.l. IT
- Product code
- KRH — Ring, Annuloplasty
- Decision date
- 2026-06-18
- Date received
- 2026-05-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K261707.pdf
Official FDA record: K261707
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.