K-number	K132519
Device name	STRYKER CUSTOMIZED MANDIBLE RECON PLATE KIT
Applicant	Stryker
Product code	JEY
Device class	Class II
Decision date	Dec 6, 2013
Decision	Substantially Equivalent
Regulation	872.4760

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Source

View the full FDA submission: accessdata.fda.gov

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STRYKER CUSTOMIZED MANDIBLE RECON PLATE KIT

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