Cleared Traditional

Tigertriever 17 Ultra Revascularization Device

K251603 · Rapid Medical , Ltd. · Neurology

Oct 2025

Decision

132d

Days

Class 2

Risk

About This 510(k) Submission

K251603 is an FDA 510(k) clearance for the Tigertriever 17 Ultra Revascularization Device, a Catheter, Thrombus Retriever (Class II — Special Controls, product code NRY), submitted by Rapid Medical , Ltd. (Yokneam, IL). The FDA issued a Cleared decision on October 6, 2025, 132 days after receiving the submission on May 27, 2025. This device falls under the Neurology review panel. Regulated under 21 CFR 870.1250.

Submission Details

510(k) Number	K251603 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 27, 2025
Decision Date	October 06, 2025
Days to Decision	132 days
Submission Type	Traditional
Review Panel	Neurology (NE)
Summary	Summary PDF

Device Classification

Product Code	NRY — Catheter, Thrombus Retriever
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 870.1250
Definition	The Device Is Intended To Restore Blood Flow By Removing Thrombus/clots In Patients Experiencing Ischemic Stroke. The Prior Clearances In This Category Have Been Limited To Simply Identifying Catheter Placed In The Peripheral, Coronary, And Neurovasculature. It Is Felt That This Is A Unique Claim And Should Not Be Combined With Previously Cleared Catheters Under A General Procode.