Medical Device Manufacturer · US , Washington , DC

Artimplant AB - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artimplant AB Orthopedic ✕

3 devices

1-3 of 3

Cleared Jun 07, 2007

ARTELON STT SPACER

Orthopedic · 331d

Cleared Jun 01, 2007

ARTELON CMC SPACER ARTHRO

Orthopedic · 325d

Cleared Sep 21, 2004

ARTELON SPACER CMC-1

Orthopedic · 251d