K-number	K222566
Device name	Zimmer Persona Personalized Knee System
Applicant	Zimmer, Inc.
Product code	MBH
Device class	Class II
Decision date	Oct 17, 2022
Decision	Substantially Equivalent
Regulation	888.3565

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Source

View the full FDA submission: accessdata.fda.gov

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Zimmer Persona Personalized Knee System

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