American Ortomed Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
American Ortomed Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1985. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by American Ortomed Corp. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jan 30, 1985
TITANIUM MITTELMEIER TYPE ACETABULAR
Orthopedic
219d
Cleared
Jan 30, 1985
UNILOC-CEMENTLESS & SELF TAP ACETABULAR
Orthopedic
204d
Cleared
Nov 19, 1984
UNILOC
Orthopedic
147d
Cleared
Mar 05, 1984
CEMENT RESTRICTOR
Orthopedic
34d
Cleared
May 12, 1982
THE ICR KNEE
Orthopedic
57d
Cleared
Jun 14, 1978
SPHERISTEM TOTAL HIP PROSTHESIS
Orthopedic
78d