K-number	K133518
Device name	MAXAN ANTERIOR CERVICAL PLATE SYSTEM
Applicant	Biomet Spine (Aka Ebi, LLC)
Product code	KWQ
Device class	Class II
Decision date	Nov 5, 2014
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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MAXAN ANTERIOR CERVICAL PLATE SYSTEM

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