Medical Device Manufacturer · US , Plymouth , MN

Medtronic Vascular, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2016

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.

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