Medtronic Core Valve, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Core Valve, LLC - FDA 510(k) Cleared Devices
Recent clearances: Medtronic Confida Brecker Guidewire
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medtronic Core Valve, LLC
2 devices