K-number	K121235
Device name	LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM
Applicant	Stryker
Product code	JEY
Device class	Class II
Decision date	Jan 9, 2014
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM

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