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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