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Hayes Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K07006136MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERTJanuary 31, 2007
K062383UNISYN HA PLASMA MODULAR HIPDecember 21, 2006
K060635CONSENSUS ACETABULAR SHELL SYSTEMApril 28, 2006
K030151CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEMApril 10, 2003
K030205CONSENSUS UNIPOLAR HEAD, COCRApril 1, 2003
K021466CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENEJuly 24, 2002
K020153CONSENSUS ACETABLAR SHELL, TI COATEDApril 15, 2002
K003649TRITON HIP SYSTEMFebruary 23, 2001
K001456CONSENSUS KNEE SYSTEMAugust 7, 2000
K983004CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TINovember 25, 1998
K964395PATIENT SPECIFIC IMPLANT (PSI) HIP FEMORAL COMPONENTJanuary 27, 1997
K953198CORTICELLOUS BONE SCREWNovember 24, 1995