K-number	K122313
Device name	STRYKER UNIVERSAL SMARTLOCK HYBRID MMF SYSTEM
Applicant	Stryker
Product code	JEY
Device class	Class II
Decision date	Oct 31, 2012
Decision	Substantially Equivalent
Regulation	872.4760

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Source

View the full FDA submission: accessdata.fda.gov

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STRYKER UNIVERSAL SMARTLOCK HYBRID MMF SYSTEM

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