Medical Device Manufacturer · US , Center Valley , PA

Aesculap - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2003

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap Orthopedic ✕

3 devices

1-3 of 3

Cleared Mar 02, 2007

S4 SPINAL SYSTEM

Orthopedic · 224d

Cleared Dec 08, 2004

BICONTACT HIP SYSTEM WITH U-CAP

Orthopedic · 30d

Cleared Aug 25, 2004

BICONTACT HIP STEM AND FEMORAL HEAD

Orthopedic · 210d