Home / Companies / Dow Corning Wright

Dow Corning Wright

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
74
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K932210ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENTSeptember 7, 1994
K932911ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENTJune 30, 1994
K934354LACEY ALL POLYETHYLENE TIBIAL COMPONENTJune 3, 1994
K932222SLT FEMORAL HEADMay 27, 1994
K932858ORTHOLOC ADVANTIM TIBIAL BASE COMPONENTFebruary 16, 1994
K930228ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREENovember 30, 1993
K925900LACEY REVISION FEMORAL COMPONENTAugust 24, 1993
K930189ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMPAugust 6, 1993
K930188ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENTAugust 3, 1993
K930190ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMPAugust 2, 1993
K926257ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENTMay 18, 1993
K920969HYDROXYLAPATITE INFINITY(R)May 5, 1993
K920968INFINITY(R) COLLARLESS/MICROTAPER TROCHANTERIC MODMay 5, 1993
K915525WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMPMay 5, 1993
K920929POLY INSERT 20 DEGREEMay 5, 1993
K925512CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATIONFebruary 12, 1993
K920593CERAMIC FEMORAL HEADAugust 31, 1992
K915448CORTICAL BONE SCREWFebruary 28, 1992
K915238TRAC-WRIGHT TRAC 10 CATHETERFebruary 19, 1992
K915350HYDROXYAPATITE INFINITY TROCHANTERIC MODULEFebruary 3, 1992