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.

510(k) submissions have been managed by Aesculap AG as regulatory consultant.

Aesculap Implant Systems is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Aesculap Implant Systems

7 devices

1-7 of 7