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FDA 510(k)

ClotTriever XL Catheter (41-102)

K-Number: K242557 · 2024-09-27

ApplicantInari Medical, Inc.
Decision Date2024-09-27
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ClotTriever XL Catheter (41-102) is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2024-09-27 under approval number K242557. 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 ClotTriever XL Catheter (41-102)?

ClotTriever XL Catheter (41-102) is a medical device that received FDA 510(k) clearance on 2024-09-27. It is manufactured by Inari Medical, Inc.. The 510(k) number is K242557.

When was ClotTriever XL Catheter (41-102) approved by the FDA?

ClotTriever XL Catheter (41-102) received FDA 510(k) clearance on 2024-09-27, under approval number K242557.

What company makes ClotTriever XL Catheter (41-102)?

ClotTriever XL Catheter (41-102) is manufactured by Inari Medical, Inc..

What is the FDA product code for ClotTriever XL Catheter (41-102)?

The FDA product code for ClotTriever XL Catheter (41-102) is QEW.

Other Devices by Inari Medical, Inc.

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Related Devices (Code: QEW)

K162970FlowTriever Retrieval/Aspiration System, Aspiration Guide Catheter, Retraction AspiratorInari Medical K161506Penumbra Aspiration SystemPenumbra, Inc. K161523INDIGO Aspiration SystemPenumbra, Inc. K160533Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc. K173470ClotTriever Thrombectomy System, ClotTriever Catheter, ClotTriever SheathInari Medical K163549ClotTriever Thrombectomy SystemInari Medical, Inc.

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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