Medical Device Manufacturer · US , Memphis , TN

Sofamor Danek USA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Total

Cleared

Denied

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

Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Sofamor Danek USA

1 devices

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