Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implant Systems - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2007

Total

Cleared

Denied

Aesculap Implant Systems has 7 FDA 510(k) cleared medical devices. Based in Center Valley, US.

Historical record: 7 cleared submissions from 2007 to 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Aesculap Implant Systems Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Aesculap Implant Systems

7 devices

1-7 of 7