K260617
- 510(k) number
- K260617
- Device name
- Tigertriever 13 Ultra Revascularization Device
- Applicant
- Rapid Medical Ltd. IL
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2026-08-28
- Date received
- 2026-02-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K260617.pdf
Official FDA record: K260617
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.