Micro Vention Inc

FDA Filings

This page includes the latest FDA filings for Micro Vention Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN K201487 Micro Vention Inc.	Traxcess 7 Mini Guidewire	2020-07-02
PMN K182602 Micro Vention Inc.	SOFIA EX Intracranial Support Catheter	2019-05-15
PMN K172014 Micro Vention, Inc.	Wedge Microcatheter	2018-04-05
PMN K151358 Micro Vention, Inc.	AZUR CX Detachable 35 Coils	2015-09-25
PMN K142449 MICRO VENTION, INC.	Headway 27 Microcatheter	2015-03-26
PMN K131482 MICRO VENTION, INC.	SOFIA DISTAL ACCESS CATHETER	2013-11-22
PMN K132083 MICRO VENTION, INC.	AZUR PURE PERIPHERAL COIL SYSTEMS, PUSHABLE 35	2013-10-28
PMN K121785 MICRO VENTION, INC.	SCEPTER C OCCLUSION BALLOON CATHETER	2012-08-10
PMN K120630 MICRO VENTION, INC.	AZUR DETACHABLE 18	2012-03-28
PMN K113698 MICRO VENTION, INC.	SCEPTER XC OCCLUSION BALLOON CATHETER	2012-01-13
PMN K110813 MICRO VENTION, INC.	HEADWAY 27 MICROCATHETER	2011-08-05

Similar & Related FDA Registered Companies

• MicroVention, Inc.
• Micro Interventional Devices, Inc.
• MicroVention, Inc., A Terumo Group Company
• MICRO INTERVENTIONAL SYSTEMS, INC.
• MicroVention, Inc.35 Enterprisealiso Viejo, CA 92656 PMA NumberP170013 Supplement NumberS010 Date Received11/09/2022 Decision Date12/09/2022 Product Code QCA  Advisory Committee Neurology Supplement Typenormal 180 Day Track No User Fee Supplement Reason Postapproval Study Protocol Expedited Review Granted? No
• MicroVention, Inc.35 Enterprisealiso Viejo, CA 92656 PMA NumberP170013 Supplement NumberS009 Date Received06/10/2022 Decision Date06/28/2022 Product Code QCA  Advisory Committee Neurology Supplement Typenormal 180 Day Track No User Fee Supplement Reason Postapproval Study Protocol Expedited Review Granted? No
• MicroVention, Inc.35 Enterpricsealiso Viejo, CA 92656 PMA NumberP180027 Supplement NumberS008 Date Received03/07/2022 Decision Date03/25/2022 Product Code OUT  Advisory Committee Neurology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• MicroVention, Inc.35 Enterpricsealiso Viejo, CA 92656 PMA NumberP180027 Supplement NumberS007 Date Received01/31/2022 Decision Date03/01/2022 Product Code OUT  Advisory Committee Neurology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No