Cintor Orthopaedic Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cintor Orthopaedic Div. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cintor Orthopaedic Div. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1980 to 1981. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cintor Orthopaedic Div. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cintor Orthopaedic Div.
7 devices
Cleared
Jun 09, 1981
RADIAL HEAD PROSTHESIS
Orthopedic
18d
Cleared
Apr 07, 1981
KNEE PROSTHESIS
Orthopedic
39d
Cleared
Feb 23, 1981
HARRIS CEMENT RESTRICTOR
Orthopedic
13d
Cleared
Feb 12, 1981
AGINSKY NAIL
Orthopedic
65d
Cleared
Jan 08, 1981
FERNORAL HIP PROSTHESIS
Orthopedic
34d
Cleared
Dec 16, 1980
ORTRON 90* HIP PROSTHESIS
Orthopedic
54d
Cleared
Dec 10, 1980
ORTHOFIX AXIALEXTERNAL FIXATION SYS.
Orthopedic
33d