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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