Medical Device Manufacturer · US , Grand Junction , CO

The S. F. Group, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

Recent clearances: DURASIL (MODIFICATION), DURASIL

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - The S. F. Group, Inc. General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Sep 03, 1996

DURASIL (MODIFICATION)

General & Plastic Surgery · 175d

Cleared Nov 22, 1995

General & Plastic Surgery · 168d