K-number	K140883
Device name	VANGUARD 360 OSSEOTI TIBIAL SLEEVE AUGMENT
Applicant	Biomet, Inc.
Product code	MBH
Device class	Class II
Decision date	Jul 30, 2014
Decision	Substantially Equivalent
Regulation	888.3565

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Source

View the full FDA submission: accessdata.fda.gov

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VANGUARD 360 OSSEOTI TIBIAL SLEEVE AUGMENT

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