ClotTriever Thrombectomy System

Catheter, Embolectomy

Inari Medical

The following data is part of a premarket notification filed by Inari Medical with the FDA for Clottriever Thrombectomy System.

Pre-market Notification Details

Device IDK192036
510k NumberK192036
Device Name:ClotTriever Thrombectomy System
ClassificationCatheter, Embolectomy
Applicant Inari Medical 9272 Jeronimo Rd., Suite 124 Irvine,  CA  92618
ContactEben Gordon
CorrespondentEben Gordon
Inari Medical 9272 Jeronimo Rd., Suite 124 Irvine,  CA  92618
Product CodeDXE  
CFR Regulation Number870.5150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2019-07-30
Decision Date2019-08-29

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