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FDA 510(k)

Tigertriever 17 Ultra Revascularization Device

K-Number: K251603 · 2025-10-06

ApplicantRapid Medical Ltd.
Decision Date2025-10-06
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Tigertriever 17 Ultra Revascularization Device is the device name listed in this FDA 510(k) record. The listed applicant is Rapid Medical Ltd.. It received FDA 510(k) clearance on 2025-10-06 under 510(k) number K251603. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tigertriever 17 Ultra Revascularization Device?

Tigertriever 17 Ultra Revascularization Device is a medical device that received FDA 510(k) clearance on 2025-10-06. The listed applicant is Rapid Medical Ltd.. The 510(k) number is K251603.

When did Tigertriever 17 Ultra Revascularization Device receive FDA 510(k) clearance?

Tigertriever 17 Ultra Revascularization Device received FDA 510(k) clearance on 2025-10-06, under 510(k) number K251603.

Who is the listed applicant for Tigertriever 17 Ultra Revascularization Device?

The FDA 510(k) record lists Rapid Medical Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tigertriever 17 Ultra Revascularization Device?

The FDA product code for Tigertriever 17 Ultra Revascularization Device is NRY.

Related Clinical Trials

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NCT05152524Distal Ischemic Stroke Treatment With Adjustable Low-profile StentrieverCOMPLETED

Other records listing Rapid Medical Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254006Drivewire 35 GuidewireK253062Tigertriever 25 Revascularization DeviceK233791Drivewire 24 GuidewireK230429Tigertriever 21 Revascularization Device, Tigertriever 17 Revascularization Device, Tigertriever 13 Revascularization DeviceK220808Tigertriever 13 Revascularization DeviceK203592Tigertriever and Tigertriever 17 Revascularization Devce

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Related Devices (Code: NRY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262398CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing setCERENOVUS, Inc.K262399Millipede SystemPerfuze, Ltd.K262391APRO 35 Swift Catheter and Alembic Aspiration TubingAlembic, LLCK260002Socrates Aspiration System (Socrates 70 Aspiration Catheter)Scientia Vascular, Inc.K250690Penumbra System (Thunderbolt Aspiration Tubing)Penumbra, Inc.K252707Zenith Aspiration Catheter; Disposable Aspiration Tubing SetSuzhou Zenith Vascular SciTech Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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