K-number	K112891
Device name	APEX REVISION KNEE SYSTEMS
Applicant	Omni Life Science, Inc.
Product code	JWH
Device class	Class II
Decision date	Feb 29, 2012
Decision	Substantially Equivalent
Regulation	888.3560

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Source

View the full FDA submission: accessdata.fda.gov

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APEX REVISION KNEE SYSTEMS

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