Medical Device Manufacturer · US , Marietta , GA

Arkin Consulting Group - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Recent clearances: LEFORTE SYSTEM BONE PLATE & SCREW

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Arkin Consulting Group Dental ✕

1 devices

1-1 of 1

Cleared May 18, 2012

LEFORTE SYSTEM BONE PLATE & SCREW