510(k) Report

Devices descending from K062201

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

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