Medical Device Manufacturer · US , Santa Rosa , CA

Medtronic Core Valve, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Medtronic Core Valve, LLC has 2 FDA 510(k) cleared medical devices. Based in Santa Rosa, US.

Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medtronic Core Valve, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic Core Valve, LLC

2 devices

1-2 of 2