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Inari Medical

FDA 510(k) & PMA Approved Devices — 25 products

Total Devices25
Categories3
Latest FDA decision2025-10-29
TypeNumberDevice NameCodeDateActions
510(k) K182531 ClotTriever Thrombectomy SystemQEW2018-10-10 View
510(k) K181694 FlowTriever Retrieval/Aspiration SystemQEW2018-07-27 View
510(k) K173672 FlowTriever Retrieval/Aspiration System, Aspiration Guide CatheterQEW2018-02-05 View
510(k) K173470 ClotTriever Thrombectomy System, ClotTriever Catheter, ClotTriever SheathQEW2017-12-04 View
510(k) K162970 FlowTriever Retrieval/Aspiration System, Aspiration Guide Catheter, Retraction AspiratorQEW2016-11-22 View

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Related Clinical Trials

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 RegistryRECRUITINGNCT06871683ClotTriever® Thrombectomy System Use-Result Survey in JapanENROLLING_BY_INVITATIONNCT07135895The ArtixASCEND StudyRECRUITINGNCT06453876Percutaneous Embolectomy, Low Dose Thrombolysis or Heparin for Intermediate High Risk Pulmonary Embolism (STRATIFY II)RECRUITING
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