Implex Corp. - FDA 510(k) Cleared Devices
65
Total
61
Cleared
0
Denied
61 devices
Cleared
Feb 03, 1997
HEDROCEL ACETABULAR RESTRICTOR
Orthopedic
223d
Cleared
Apr 05, 1996
IMPLEX CERAMIC HEAD
Orthopedic
148d
Cleared
Jul 06, 1995
F-230 POROUS FEMORAL HIP STEM (CEMENTLESS)
Orthopedic
458d
Cleared
Sep 23, 1994
IMPLEX CEMENT RESTRICTOR SYSTEM
Orthopedic
72d
Cleared
Jul 13, 1994
F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM
Orthopedic
211d
Cleared
May 12, 1994
IMPLEX A-230 POROUS ACETABULAR CUP SYST. CEMENTED
Orthopedic
331d
Cleared
May 03, 1994
IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS
Orthopedic
322d
Cleared
Feb 07, 1994
IMPLEX ACETABULAR CUP SCREW SYSTEM
Orthopedic
335d
Cleared
Oct 15, 1993
H-220 PRESS-FIT ACETABULAR CUP SYSTEM
Orthopedic
312d
Cleared
May 26, 1993
H-110 ACETABULAR CUP SYSTEM
Orthopedic
161d
Cleared
May 12, 1993
IMPLEX H-110 AND H-120 CEMENTED HIP STEM SYSTEM
Orthopedic
202d