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Medtronic Vascular

FDA 510(k) & PMA Approved Devices — 474 products

Total Devices474
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K232570 Steerant™ Super Stiff GuidewireDQX2023-10-24 View
510(k) K232190 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide CatheterDQY2023-08-22 View
510(k) K230156 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide CatheterDQY2023-06-30 View
510(k) K220773 Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)MAV2022-04-13 View
510(k) K192296 Medtronic 6F Taiga Guiding CatheterDQY2019-09-20 View
510(k) K173515 Admiral XtremeLIT2018-04-12 View
510(k) K162097 InTRAkitDYB2016-11-17 View
510(k) K162027 TRAcelet Compression DeviceDXC2016-10-21 View
510(k) K161287 DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA Angio-Kit, DxTerity TRA EZ-PakDQO2016-08-19 View
510(k) K123990 SENTRANT INTRODUCER SHEATH WITH HYDROPHILIC COATINGDYB2013-04-26 View
510(k) K123358 PACIFIC PLUSLIT2013-01-29 View
510(k) K101777 PIONEER PLUS CATHETER, MODEL PLUS 120PDU2010-07-23 View
510(k) K091582 GTX GUIDEWIRE, MODELS TBD-GTX 1, 3,6,9,12, 15DQX2009-12-04 View
510(k) K083422 6F TAIGA GUIDING CATHETERDQY2009-02-06 View
510(k) K082873 MEDTRONIC ANGIOGRAPHIC GUIDE WIRESDQX2009-02-06 View
510(k) K081573 MEDTRONIC EXPORT AP CATHETERDXE2008-06-27 View
510(k) K062264 COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEMFGE2007-11-08 View
510(k) K071253 AFFINITY PEDIATRIC ARTERIAL FILTER, MODEL S4014 AND WITH CARMEDA BIOACTIVE SURFACE, MODEL CB4014DTM2007-07-03 View
510(k) K070288 CARDIOBLATE MONOPOLAR PEN, 60813, CARDIOBLATE MONOPOLAR XL, 60814OCL2007-06-18 View
510(k) K070311 CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261GEI2007-04-24 View
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