K-number	K242543
Device name	Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)
Applicant	Zimmer, Inc.
Product code	MBH
Device class	Class II
Decision date	Nov 22, 2024
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)

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