K-number	K061002
Device name	MAXIMA ANTERIOR CERVICAL PLATE SYSTEM
Applicant	U&I Corp.
Product code	KWQ
Device class	Class II
Decision date	Nov 15, 2006
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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MAXIMA ANTERIOR CERVICAL PLATE SYSTEM

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