510(k) Report

Devices descending from K050139

14 later devices reach Modification to: Export Catheter through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K052523Proxis SystemVelocimed, Inc.20062—
+1K053372Lbi Catheter SystemLumen Biomedical, Inc.200610—
+2K0737006F Proxis SystemSt. Jude Medical, Inc.20080—
+2K073563Modification to Proxis SystemSt Jude Medical20080—
+2K071529Xtract Catheter SystemLumen Biomedical, Inc.200791
+3K113757Aspire Max Aspiration CatheterControl Medical Technology, LLC20125—
+3K082348Fibernet Embolic Protection SystemLumen Biomedical, Inc.200812
+3K080901Lbi Embolectomy SystemLumen Biomedical, Inc.20086—
+4K220780ROVO Mechanical Thrombectomy Device2mg, Inc.20231—
+4K200629Aspire Mechanical Aspirator GControl Medical Technology20200—
+4K200871Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical AspiratorControl Medical Technology20201—
+4K111987Fibernet Embolic Protection DeviceLumen Biomedical, Inc.20110—
+5K253730RoVo Mechanical Thrombectomy SystemVerge Medical, Inc.20260—
+5K250013VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S…Control Medical Technology, Inc. / Dba Ventiv Scientific20250—