FDA 510(k) Applications Submitted by HAYES MEDICAL, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K964395 |
11/04/1996 |
PATIENT SPECIFIC IMPLANT (PSI) HIP FEMORAL COMPONENT |
HAYES MEDICAL, INC. |
K983004 |
08/28/1998 |
CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI |
HAYES MEDICAL, INC. |
K070061 |
01/05/2007 |
36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT |
HAYES MEDICAL, INC. |
K060635 |
03/10/2006 |
CONSENSUS ACETABULAR SHELL SYSTEM |
HAYES MEDICAL, INC. |
K062383 |
08/15/2006 |
UNISYN HA PLASMA MODULAR HIP |
HAYES MEDICAL, INC. |
K030151 |
01/15/2003 |
CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEM |
HAYES MEDICAL, INC. |
K020153 |
01/16/2002 |
CONSENSUS ACETABLAR SHELL, TI COATED |
HAYES MEDICAL, INC. |
K030205 |
01/21/2003 |
CONSENSUS UNIPOLAR HEAD, COCR |
HAYES MEDICAL, INC. |
K021466 |
05/07/2002 |
CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENE |
HAYES MEDICAL, INC. |
K001456 |
05/09/2000 |
CONSENSUS KNEE SYSTEM |
HAYES MEDICAL, INC. |
K003649 |
11/27/2000 |
TRITON HIP SYSTEM |
HAYES MEDICAL, INC. |
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