K260498
- 510(k) number
- K260498
- Device name
- TriMemo SEMIRIGID ANNULOPLASTY RING
- Applicant
- Corcym S.r.l. IT
- Product code
- KRH — Ring, Annuloplasty
- Decision date
- 2026-04-14
- Date received
- 2026-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K260498.pdf
Official FDA record: K260498
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.