FDA 510(k) Applications Submitted by GRAHAM CUTHBERT

FDA 510(k) Number Submission Date Device Name Applicant
K071676 06/19/2007 EXACTECH NOVATION CROWN CUP CONSTRAINED LINERS AND RINGS EXACTECH, INC.
K082022 07/16/2008 OPTETRAK 9MM CRUCIATE RETAINING TIBIAL INSERT, SLOPE ++ EXACTECH, INC.
K093430 11/03/2009 EXACTECH EQUINOXE XL KEELED GLENOID, PEGGED GLENOID, EXACTECH EQUINOXE CAGE, GLENOID CONTD. EXACTECH, INC.
K073688 12/28/2007 EQUINOXE REVERSE SHOULDER SYSTEM FRACTURE HUMERAL ADAPTER TRAY AND LOCKING SCREW EXACTECH, INC.
K100269 01/29/2010 NOVATION CROWN CUP GXL LINERS EXACTECH, INC.
K110706 03/14/2011 EXACTECH EQUINOXE CUFF TEAR ARTHROPLASTY (CTA) HEAD EXACTECH, INC.
K111379 05/17/2011 EQUINOXE UHMWPE 12* POSTERIOR AUGMENT PEGGED GLENOID, SMALL / MEDIUM / LARGE / EXTRA-LARGE, LEFT / RIGHT EXACTECH, INC.
K101909 07/08/2010 EXACTECH EQUINOXE, PLATFORM FRACTURE STEM EXACTECH, INC.
K102951 10/05/2010 EXACTECH EQUINOX FIXED ANGLE REPLICATOR PLATE (0MM,1.5MM,4.5MM), HUMERAL HEAD-SHORT (44MM,47MM), GLENOSPHERE (38MM,42MM) EXACTECH, INC.
K083392 11/17/2008 NOVATION 12/14 CEMENTED FEMORAL STEMS EXACTECH, INC.


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