Tigertriever 17 Ultra Revascularization Device— 510(k) K251603

Substantially Equivalent

Rapid Medical , Ltd.

FDA 510(k) clearance K251603 for Tigertriever 17 Ultra Revascularization Device, Substantially Equivalent on 2025-10-06. Applicant: Rapid Medical , Ltd..

Clearance details

Applicant: Rapid Medical , Ltd.
Product code: Code NRY
Advisory panel: Cardiovascular
Date received: 2025-05-27
Decision date: 2025-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yokneam, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code NRY

product code NRY

Death: 411
Injury: 1,712
Malfunction: 1,855
Total: 3,978

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.