Praxim S.A is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Praxim S.A - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Praxim S.A has 4 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 4 cleared submissions from 2006 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Praxim S.A Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Praxim S.A
4 devices
Cleared
Dec 10, 2007
TOTAL HIP SURGETICS NAVIGATION SYSTEM
Neurology
117d
Cleared
Aug 21, 2006
UNI KNEE SURGETICS NAVIGATION SYSTEM
Neurology
25d
Cleared
Apr 10, 2006
SURGETICS ORTHO OSTEOLOGICS NAVIGATION SYSTEM
Neurology
111d
Cleared
Apr 10, 2006
TOTAL KNEE SURGETICS NAVIGATION SYSTEM
Neurology
66d