Omnlife Science
6 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| OMNI Interface Acetabular System (K142201) | Omnlife Science | 2015-01-26 |
| APEX MODULAR ACCTABULAR CUP (NOW NAMED APEX INTERFACE ACETABULAR SYSTEM) (K112779) | Omnlife Science | 2011-12-02 |
| APEX KNEE MODULAR TIBIA SYSTEM (K101994) | Omnlife Science | 2010-09-28 |
| APEX MODULAR HEAD, SIZE 28 ,32, 26 AND 40 MM+10.5 OFFSET, MODELS 302810, 303210,303610,304010 (K101575) | Omnlife Science | 2010-06-30 |
| APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX (OD 38 TO 43MM), H3-828XX (OD44 TO 60MM) (K100151) | Omnlife Science | 2010-05-28 |
| MODIFICATION TO: APEX KNEE SYSTEM (K073602) | Omnlife Science | 2008-02-14 |
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Every clearance here is in the API, with alerts when new ones post.