Atrix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atrix - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Atrix has 2 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 2 cleared submissions from 1985 to 1986. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Atrix Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Atrix
2 devices