Implant Technology, Inc. - FDA 510(k) Cleared Devices
13
Total
11
Cleared
0
Denied
Implant Technology, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Walker, US.
Historical record: 11 cleared submissions from 1983 to 1995.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Jan 11, 1995
HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESIS
Orthopedic
1013d
Cleared
May 28, 1992
LSF HA COATED FEMORAL HIP
Orthopedic
164d
Cleared
Mar 25, 1992
LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUP
Orthopedic
83d
Cleared
Nov 07, 1991
LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP
Orthopedic
86d
Cleared
Aug 09, 1990
LSF CEMENTED FEMORAL HIP
Orthopedic
49d
Cleared
May 22, 1990
LSF(TM) TOTAL HIP SYSTEM
Orthopedic
55d
Cleared
May 02, 1989
IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR
Orthopedic
48d
Cleared
Dec 09, 1988
MODIFIED LSF TOTAL HIP SYSTEM
Orthopedic
49d
Cleared
Nov 22, 1988
LSF (R) TOTAL HIP SYSTEM - BIPOLAR COMPONENT
Orthopedic
116d
Cleared
Jun 11, 1986
LSF* TOTAL HIP SYSTEM
Orthopedic
177d
Cleared
Apr 30, 1984
COMMUNI-TRACH TUBE
Anesthesiology
14d
Cleared
Jul 07, 1983
TRACHEOSTOMY TUBE
Anesthesiology
56d
Cleared
Jan 08, 1983
COMMUNITRACH TUBE
Anesthesiology
64d