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FDA 510(k)

Zimmer Persona Personalized Knee System

K-Number: K172524 · 2018-05-17

ApplicantZimmer, Inc.
Decision Date2018-05-17
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Zimmer Persona Personalized Knee System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2018-05-17 under approval number K172524. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Zimmer Persona Personalized Knee System?

Zimmer Persona Personalized Knee System is a medical device that received FDA 510(k) clearance on 2018-05-17. It is manufactured by Zimmer, Inc.. The 510(k) number is K172524.

When was Zimmer Persona Personalized Knee System approved by the FDA?

Zimmer Persona Personalized Knee System received FDA 510(k) clearance on 2018-05-17, under approval number K172524.

What company makes Zimmer Persona Personalized Knee System?

Zimmer Persona Personalized Knee System is manufactured by Zimmer, Inc..

What is the FDA product code for Zimmer Persona Personalized Knee System?

The FDA product code for Zimmer Persona Personalized Knee System is MBH.

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Official Source

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