Artos Medical Products GmbH is one of 12960 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Artos Medical Products GmbH - FDA 510(k) Cleared Devices
Recent clearances: SC, CEMENTLESS HIP SYSTEM, CHROME COBALT BALL HEAD, CPS, CEMENTED CUP SYSTEM
4
Total
4
Cleared
0
Denied
Artos Medical Products GmbH has 4 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 4 cleared submissions from 1996 to 1996. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Artos Medical Products GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Artos Medical Products GmbH
4 devices