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Kinamed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
33
Inspections
6
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K122049NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEMApril 5, 2013
K072250SUPERCABLE GRIP AND PLATE SYSTEMNovember 9, 2007
K050897NAVIPRO SHOULDER SOFTWARE MODULEMay 24, 2005
K033668NAVIPRO KNEE SOFTWARE MODULEMarch 11, 2004
K032950GEM INSET PATELLAR COMPONENTDecember 19, 2003
K030256ISO-ELASTIC CERCLAGE SYSTEMOctober 21, 2003
K020764NAVIPROJune 3, 2002
K013982KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANTMay 21, 2002
K010101GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEMMay 17, 2001
K003347ORTHOPILOTFebruary 23, 2001
K994214GEM KNEE SYSTEMJuly 19, 2000
K982927QUICK TAP SELF DRILLING SCREWSeptember 8, 1998
K964362KINAMED PROFIX SYSTEMJanuary 16, 1997
K954219REALITY LONG STEM HIP SYSTEMDecember 4, 1995
K954213ATH FULL PROFILE ACETABULAR CUP SYSTEMOctober 25, 1995
K922247KINAMED REALITY TOTAL HIP SYSTEMMarch 30, 1994
K920290KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALLNovember 3, 1992
K920219KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALLOctober 30, 1992
K922421KINAMED ATH-POROUS AND ATH-POROUS LONG TOTAL HIPOctober 15, 1992
K915309KINAMED 22MM BIOCERAM-Z TOTAL HIP FEMORAL BALLFebruary 19, 1992