Medtronic Vascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Vascular - FDA 510(k) Cleared Devices
Recent clearances: Steerant™ Super Stiff Guidewire, 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter, 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
475
Total
453
Cleared
0
Denied
Medtronic Vascular has 453 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Last cleared in 2023. Active since 1977.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Underwriters Laboratories, Inc..
FDA 510(k) Regulatory Record - Medtronic Vascular
475 devices
Cleared
Oct 24, 2023
Steerant™ Super Stiff Guidewire
Cardiovascular
61d
Cleared
Aug 22, 2023
6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter
Cardiovascular
29d
Cleared
Jun 30, 2023
5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide...
Cardiovascular
162d
Cleared
Apr 13, 2022
Everest 20 Inflation Device and 3-way Stopcock (AC2200)
Cardiovascular
28d
Cleared
Sep 20, 2019
Medtronic 6F Taiga Guiding Catheter
Cardiovascular
28d
Cleared
Apr 12, 2018
Admiral Xtreme
Cardiovascular
149d
Cleared
Nov 17, 2016
InTRAkit
Cardiovascular
111d
Cleared
Oct 21, 2016
TRAcelet Compression Device
Cardiovascular
91d
Cleared
Aug 19, 2016
DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA...
Cardiovascular
102d
Cleared
Mar 26, 2014
TOTAL ACROSS
Cardiovascular
128d
Cleared
Apr 26, 2013
SENTRANT INTRODUCER SHEATH WITH HYDROPHILIC COATING
Cardiovascular
121d
Cleared
Jan 29, 2013
PACIFIC PLUS
Cardiovascular
90d
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