K-number	K130126
Device name	SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM
Applicant	Biomet, Inc.
Product code	MBF
Device class	Class II
Decision date	Aug 6, 2013
Decision	Substantially Equivalent
Regulation	888.3670

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View the full FDA submission: accessdata.fda.gov

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SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM

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