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FDA 510(k)

Persona Personalized Knee System

K-Number: K193223 · 2020-01-24

ApplicantZimmer, Inc.
Decision Date2020-01-24
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Persona Personalized Knee System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2020-01-24 under approval number K193223. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Persona Personalized Knee System?

Persona Personalized Knee System is a medical device that received FDA 510(k) clearance on 2020-01-24. It is manufactured by Zimmer, Inc.. The 510(k) number is K193223.

When was Persona Personalized Knee System approved by the FDA?

Persona Personalized Knee System received FDA 510(k) clearance on 2020-01-24, under approval number K193223.

What company makes Persona Personalized Knee System?

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

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

The FDA product code for Persona Personalized Knee System is JWH.

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Official Source

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