Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implant System, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2007

18

Total

18

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap Implant System, Inc. Neurology ✕

1 devices

1-1 of 1

Cleared May 23, 2008

ORTHOPILOT NEXT GENERATION, MODEL FS101-FS106

Neurology · 85d