Medical Device Manufacturer · US , Center Valley , PA

Aesculap - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2003

Recent clearances: AESCULAP STERILCONTAINER S, S4 SPINAL SYSTEM, AESCULAP STERILCONTAINER SYSTEM

View 10 510(k) Devices ↓

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap Neurology ✕

3 devices

1-3 of 3

Cleared Jul 11, 2006

MINOP DISPOSABLE INTRODUCER 10F, MODEL ME010

Neurology · 78d

Cleared Jun 17, 2004

CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM

Neurology · 76d

Cleared May 09, 2003

AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)

Neurology · 39d