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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 the device name listed in this FDA 510(k) record. The listed applicant is Inari Medical, Inc.. It received FDA 510(k) clearance on 2024-09-27 under 510(k) 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. The listed applicant is Inari Medical, Inc.. The 510(k) number is K242557.

When did ClotTriever XL Catheter (41-102) receive FDA 510(k) clearance?

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

Who is the listed applicant for ClotTriever XL Catheter (41-102)?

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

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

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

Related Clinical Trials

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.

NCT05701917DEFIANCE: RCT of ClotTriever System Versus Anticoagulation In Deep Vein ThrombosisRECRUITINGNCT06055920The PEERLESS II StudyACTIVE_NOT_RECRUITINGNCT06394739RevCore for In Stent ThrombosisRECRUITINGNCT06495996The Protrieve PROTECTOR StudyCOMPLETEDNCT06588634The PERSEVERE StudyRECRUITINGNCT06600542Inari VISION RegistryRECRUITING

Other records listing Inari Medical, Inc. 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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