K-number	K123459
Device name	ZIMMER PERSONA TM PERSONALIZED KNEE SYSTEM
Applicant	Zimmer, Inc.
Product code	MBH
Device class	Class II
Decision date	Feb 22, 2013
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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ZIMMER PERSONA TM PERSONALIZED KNEE SYSTEM

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