FDA 510(k) Applications Submitted by MARITZA ELIAS
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K060107 |
01/13/2006 |
MODIFICATION TO: EXACTECH ZIRAMIC ZIRCONIA 12/14 FEMORAL HEADS |
EXACTECH, INC. |
K110327 |
02/03/2011 |
LDR SPINE ROI-A INTERBODY FUSION SYSTEM |
LDR SPINE USA |
K070479 |
02/20/2007 |
EXACTECH NOVATION CROWN CUP AND LINERS |
EXACTECH, INC. |
K051335 |
05/23/2005 |
ACUMATCH 12/14 PRESS-FIT FEMORAL STEMS |
EXACTECH, INC. |
K061454 |
05/25/2006 |
EXACTECH EQUINOXE SHOULDER STEMS |
EXACTECH, INC. |
K081622 |
06/10/2008 |
UNIVERSAL CLAMP STAINLESS STEEL SYSTEM |
ABBOTT SPINE, INC. |
K061668 |
06/14/2006 |
OPTECURE +CCC |
EXACTECH, INC. |
K051682 |
06/23/2005 |
EXACTECH 12/14 ALUMINA FEMORAL HEADS 36 MM |
EXACTECH, INC. |
K052787 |
10/03/2005 |
ACUMATCH 12/14 C-SERIES CEMENTED FEMORAL STEMS (SIZE 1-6), ACUMATCH 12/14 L-SERIES CEMENTED FEMORAL STEMS (SIZE 1-5) |
EXACTECH, INC. |
K123134 |
10/05/2012 |
EASYSPINE SYSTEM |
LDR SPINE USA INC. |
K063279 |
10/31/2006 |
NOVATION SPLINED RDD FEMORAL STEMS |
EXACTECH, INC. |
K113285 |
11/07/2011 |
LDR SPINE USA AVENUE L INTERBODY FUSION |
LDR SPINE USA INC. |
K073202 |
11/13/2007 |
ARDIS SPACER |
ABBOTT SPINE, INC. |
K063685 |
12/12/2006 |
OPTECURE; OPTECURE + CCC |
EXACTECH, INC. |
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