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FDA 510(k)

InThrill™ Thrombectomy System

K-Number: K250421 · 2025-05-12

Decision Date2025-05-12
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

InThrill™ Thrombectomy System is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2025-05-12 under approval number K250421. 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 InThrill™ Thrombectomy System?

InThrill™ Thrombectomy System is a medical device that received FDA 510(k) clearance on 2025-05-12. It is manufactured by Inari Medical, Inc.. The 510(k) number is K250421.

When was InThrill™ Thrombectomy System approved by the FDA?

InThrill™ Thrombectomy System received FDA 510(k) clearance on 2025-05-12, under approval number K250421.

What company makes InThrill™ Thrombectomy System?

InThrill™ Thrombectomy System is manufactured by Inari Medical, Inc..

What is the FDA product code for InThrill™ Thrombectomy System?

The FDA product code for InThrill™ Thrombectomy System is QEW.

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Official Source

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