K-number	K060303
Device name	VANGUARD PS OPEN BOX POROUS FEMORAL COMPONENTS
Applicant	Biomet Manufacturing Corp
Product code	MBH
Device class	Class II
Decision date	Mar 30, 2006
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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VANGUARD PS OPEN BOX POROUS FEMORAL COMPONENTS

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