Medical Device Manufacturer · US , Plainview , NY

George Tiemann & Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - George Tiemann & Co. Orthopedic ✕

1 devices

1-1 of 1

Cleared Dec 09, 1985

TITANIUIM BONE SCREW

Orthopedic · 83d