Medtronic Vascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Vascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Heli-FX EndoAnchor System
5
Total
5
Cleared
0
Denied
Medtronic Vascular, Inc. has 5 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 5 cleared submissions from 2016 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic Vascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronic Vascular, Inc.
5 devices
Cleared
Nov 21, 2018
Heli-FX EndoAnchor System
Cardiovascular
28d
Cleared
Dec 20, 2017
Sentrant Introducer Sheath with Hydrophilic Coating
Cardiovascular
181d
Cleared
Jun 16, 2017
SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque...
Cardiovascular
144d
Cleared
Jun 13, 2017
Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor Cassette
Cardiovascular
29d
Cleared
Oct 14, 2016
HawkOne Directional Atherectomy System
Cardiovascular
151d