Medical Device Manufacturer · US , Walker , MI

Medtronic Vascular - FDA 510(k) Cleared Devices

475 submissions · 453 cleared · Since 1977
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.

510(k) submissions have been managed by Medtronic Vascular as regulatory consultant.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Medtronic Vascular
475 devices
1-12 of 475

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