Medical Device Manufacturer · US , Santa Rosa , CA

Medtronic Endovascular Innovations - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Total

Cleared

Denied

Medtronic Endovascular Innovations has 1 FDA 510(k) cleared medical devices. Based in Santa Rosa, US.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medtronic Endovascular Innovations Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic Endovascular Innovations

1 devices

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