K-number	K110533
Device name	STRYKER PATIENT SPECIFIC CUTTING GUIDE
Applicant	Stryker Corp.
Product code	MBH
Device class	Class II
Decision date	May 19, 2011
Decision	Substantially Equivalent
Regulation	888.3565

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Source

View the full FDA submission: accessdata.fda.gov

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STRYKER PATIENT SPECIFIC CUTTING GUIDE

Everything you need for a 510(k) submission. Nothing you don't.