K-number	K121862
Device name	REX ANTERIOR CERVICAL PLATE SYSTEM
Applicant	Dio Medical Co., Ltd.
Product code	KWQ
Device class	Class II
Decision date	Oct 31, 2012
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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REX ANTERIOR CERVICAL PLATE SYSTEM

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