K-number	K132873
Device name	VANGUARD XP KNEE SYSTEM
Applicant	Biomet, Inc.
Product code	MBH
Device class	Class II
Decision date	Dec 11, 2013
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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