K-number	K143336
Device name	Biomet Microfixation OmniMax MMF System
Applicant	Biomet Microfixation
Product code	JEY
Device class	Class II
Decision date	Apr 1, 2015
Decision	Substantially Equivalent
Regulation	872.4760

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Source

View the full FDA submission: accessdata.fda.gov

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Biomet Microfixation OmniMax MMF System

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