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 General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jul 17, 2003

MONOPLUS POLY-P-DIOXANONE MONOFILAMENT ABSORBABLE SURGICAL SUTURE

General & Plastic Surgery · 91d