Techmedica, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
31
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933935CKS POROUS COATED FEMORAL COMPONENTOctober 11, 1994
K932017TECHMEDICA CONTINUUM HIP WITH HA COATINGSeptember 1, 1994
K931929TECHMEDICA CONTINUUM HIP SYSTEMMarch 29, 1994
K926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMFebruary 1, 1994
K925420TECHMEDICA STANDARD BIPOLAR SYSTEMSeptember 28, 1993
K923808MULLER STRAIGHT STEM FEMORAL PROSTHESISJuly 27, 1993
K926579TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCREApril 6, 1993
K911058TECHMEDICA CAD/CAM CUSTOM HIPFebruary 23, 1993
K925181TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUPFebruary 5, 1993
K920080CONTINUUM KNEE SYSTEMSeptember 1, 1992
K921458TMP MICROPLATING SYSTEMJuly 17, 1992
K921801MODIFICATION TECHMEDICA MP (MINIPLATING) SYSTEMJuly 15, 1992
K921131CKS OSCILLATING SAW BLADEJune 8, 1992
K914072CONTINUUM KNEE SYSTEM (CKS)February 18, 1992
K915187CANCELLOUS BONE-L.P. AND CORTICAL BONE SCREWDecember 19, 1991
K905024TMP MANDIBULAR COMPRESSION SYSTEMJune 24, 1991
K903286CONTINUUM KNEE SYSTEM (CKS)-MODIFICATIONOctober 12, 1990
K901457CONTINUUM KNEE SYSTEM (CKS)June 20, 1990
K900619CAAS UNICOMPARMENTAL KNEE SYSTEMJune 11, 1990
K896542ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))February 15, 1990