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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