Medical Device Manufacturer · US , Memphis , TN

Medtronic Soafamor Danek - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

Total

Cleared

Denied

Medtronic Soafamor Danek has 1 FDA 510(k) cleared medical devices. Based in Memphis, US.

Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Medtronic Soafamor Danek

1 devices

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