510(k) Report

Devices descending from K053195

14 later devices reach Spiderx Embolic Protection Device through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K062201Spiderx Embolic Protection DeviceEv3, Inc.200613—
+2K063785Spiderfx Embolic Protection DeviceEv3, Inc.200712—
+3K090364Extra Pta Balloon Catheter with Embolic Protection FeatureAngioslide, Ltd.201010—
+3K073523Interceptor Plus Coronary Filter SystemsMedtronic, Inc.20080—
+4K111010Spiderfx Embolic Protection DeviceEv3, Inc.20114—
+4K111750Extra Pta Balloon Catheter with Embolic Capture Feature; Proteus Pta Balloon Catheter…Angioslide, Ltd.20115—
+5K181529Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic ProtectionContego Medical, LLC20180—
+5K180023WirionGardia Medical, Ltd.20182—
+5K120164Proteus Pta Balloon Catheter with Embolic Capture FeatureAngioslide, Ltd.20120—
+5K120805Proteus Pta Balloon Catheter with Embolic Capture FeatureAngioslide, Ltd.20123—
+6K200198WirionCardiovascular Systems, Inc.20201—
+6K133043Proteus Pta Balloon Catheter with Embolic Capture FeatureAngioslide, Ltd.20132—
+7K210282WIRION Embolic Protection SystemCardiovascular Systems, Inc.20210Class I
+7K172494PROTEUS PTA Balloon Catheter with Embolic Capture FeatureAngioslide, Ltd.20171—