FDA 510(k) Applications Submitted by OMNI LIFE SCIENCE, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K131472 05/22/2013 APEX KNEE MODULAR TIBIA SYSTEM OMNI LIFE SCIENCE, INC.
K191765 07/01/2019 OMNI TiN Coated Apex KneeÖ System OMNI life science, Inc.
K112891 09/30/2011 APEX REVISION KNEE SYSTEMS OMNI LIFE SCIENCE, INC.
K060072 01/09/2006 MONOBLOCK PRESS-FIT HIP STEM OMNI LIFE SCIENCE, INC.
K060192 01/25/2006 APEX KNEE SYSTEM OMNI LIFE SCIENCE, INC.
K073150 11/08/2007 APEX-LNK POLY ACETABULAR CUP LINERS OMNI LIFE SCIENCE, INC.
K100555 03/01/2010 APEX-LNK ACETABULAR INSERT, E, APEX-LNK ACETABULAR INSERT, F, APEX-LNK OMNI LIFE SCIENCE, INC.
K101451 05/25/2010 APEX MODULE HIP SYSTEM BIOLOX DELTA FEMORAL HEAD OMNI LIFE SCIENCE, INC.
K101976 07/13/2010 INTERFACE ACETABULAR SYSTEM, ACETABULAR INSERT +4 OFFSET OMNI LIFE SCIENCE, INC.
K102578 09/08/2010 APEX PS KNEE SYSTEM OMNI LIFE SCIENCE, INC.
K094017 12/29/2009 TIBIAL BASEPLATE AUGMENT MODEL KC-22118, KC-22128, KC-22138, KC-22148, KC-22158 OMNI LIFE SCIENCE, INC.
K080842 03/25/2008 APEX KNEE SYSTEM, MODEL KC-230XY, KC-240XY [ NO HOLES, 2 HOLES] OMNI LIFE SCIENCE, INC.
K090845 03/27/2009 APEX ARC HIP STEM OMNI LIFE SCIENCE, INC.
K092443 08/10/2009 INTERFACE ACETABULAR CUP LINERS OMNI LIFE SCIENCE, INC.
K082468 08/27/2008 APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX AND H3-828YY, XX=OD IN [MM] (38-43), YY=OD IN [MM](44-60) OMNI LIFE SCIENCE, INC.


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