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FDA 510(k)

Liberant Thrombectomy System

K-Number: K250787 · 2025-06-11

ApplicantMedtronic, Ireland
Decision Date2025-06-11
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Liberant Thrombectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Ireland. It received FDA 510(k) clearance on 2025-06-11 under 510(k) number K250787. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Liberant Thrombectomy System?

Liberant Thrombectomy System is a medical device that received FDA 510(k) clearance on 2025-06-11. The listed applicant is Medtronic, Ireland. The 510(k) number is K250787.

When did Liberant Thrombectomy System receive FDA 510(k) clearance?

Liberant Thrombectomy System received FDA 510(k) clearance on 2025-06-11, under 510(k) number K250787.

Who is the listed applicant for Liberant Thrombectomy System?

The FDA 510(k) record lists Medtronic, Ireland as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Liberant Thrombectomy System?

The FDA product code for Liberant Thrombectomy System is QEW.

Other records listing Medtronic, Ireland as applicant

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Related Devices (Code: QEW)

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.

K261523Vertex™ Thrombectomy SystemJupiter EndovascularK260599INDIGO® Aspiration System – INDIGO LinkPenumbra, Inc.K260028CLEANER™ Vac Thrombectomy System, CLEANER™ Vac Aspiration Catheter with Handpiece, CLEANER™ Vac Aspiration CanisterArgon Medical Devices, Inc.K251949INDIGO® Aspiration System - Lightning Flash Aspiration Tubing with LINKPenumbra, Inc.K253730RoVo Mechanical Thrombectomy SystemVerge Medical, Inc.K251207Sangria™ Thrombectomy SystemAvantec Vascular Corporation

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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