The Deca Co. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
The Deca Co. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1982 to 1987. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by The Deca Co. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Jul 17, 1987
FLEXIBLE FASCICULATED BONE PLATE
Dental
193d
Cleared
Mar 26, 1987
INTRAMEDULLARY NAIL
Orthopedic
80d
Cleared
Dec 24, 1986
FASCICULATED I ROD
Orthopedic
126d
Cleared
Dec 24, 1986
FASCICULATED BOAT ROD
Orthopedic
124d
Cleared
Dec 24, 1986
FASCICULATED S ROD
Orthopedic
121d
Cleared
Aug 11, 1986
INTRAMEDULLARY ROD
Orthopedic
133d
Cleared
Feb 04, 1986
FASCILULATED NAIL
Orthopedic
109d
Cleared
Mar 01, 1983
INTRAMEDULLARY ROD
Orthopedic
49d
Cleared
Jan 29, 1982
HIP PIN
Orthopedic
65d