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Omnlife Science

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K112779	APEX MODULAR ACCTABULAR CUP (NOW NAMED APEX INTERFACE ACETABULAR SYSTEM)	LPH	2011-12-02	View
510(k)	K101994	APEX KNEE MODULAR TIBIA SYSTEM	JWH	2010-09-28	View
510(k)	K101575	APEX MODULAR HEAD, SIZE 28 ,32, 26 AND 40 MM+10.5 OFFSET, MODELS 302810, 303210,303610,304010	LPH	2010-06-30	View
510(k)	K100151	APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX (OD 38 TO 43MM), H3-828XX (OD44 TO 60MM)	KWY	2010-05-28	View
510(k)	K073602	MODIFICATION TO: APEX KNEE SYSTEM	JWH	2008-02-14	View

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