510(k) Report

Devices descending from K030779

10 later devices reach 5F Medtronic Launcher Guide Catheter through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K140034Surefire Guiding CatheterSurefire Medical, Inc.20142—
+1K120585Convey Guiding CatheterPendracare International, B.V.20122—
+1K103386Medtronic Vascular - Hub Material Modification to the 5F and 8F Launcher (R) Guide…Medtronic, Inc.201111
+1K0624205F Sherpa Active NX Guide CatheterMedtronic Vascular20062—
+2K250972Primum Hydrophilic Guiding CatheterPendracare20250—
+2K233858TriSalus TriGuideTM Guiding CatheterTrisalus Life Sciences20230—
+2K162359Surefire Guiding CatheterSurefire Medical, Inc.20160—
+2K141529Alviguide Blue+ Interventional Cardiology Guiding CatheterAlvimedica Tibbi Urunler Sanayi VE Dis Ticaret A.S20140—
+2K1326735F & 6F Launcher Guide Catheter, 5F Sherpa Active NX Guide Catheter, 6F Z4 Guiding…Medtronic, Inc.20130Class I
+2K132197Convey 7F Guiding Catheter, Convey 8F Guiding CatheterPendracare International, B.V.20130—