K-number	K153657
Device name	Vanguard XP Knee System
Applicant	Biomet, Inc.
Product code	MBH
Device class	Class II
Decision date	May 10, 2016
Decision	Substantially Equivalent
Regulation	888.3565

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Source

View the full FDA submission: accessdata.fda.gov

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Vanguard XP Knee System

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