Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implants Systems, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Recent clearances: Modulift Vertebral Body Replacement (VBR) System

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap Implants Systems, Inc. Orthopedic ✕

1 devices

1-1 of 1

Cleared Nov 20, 2017

Modulift Vertebral Body Replacement (VBR) System

Orthopedic · 138d