Medical Device Manufacturer · US , Fr. Myers , FL

Arthro-Dif - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Recent clearances: ACROSSPINE PEDICLE SCREW SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Arthro-Dif Orthopedic ✕

1 devices

1-1 of 1

Cleared Dec 30, 2014

ACROSSPINE PEDICLE SCREW SYSTEM

Orthopedic · 189d