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FDA 510(k)

Zimmer® Persona® Personalized Knee System

K-Number: K243293 · 2024-12-20

ApplicantZimmer Biomet
Decision Date2024-12-20
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Zimmer® Persona® Personalized Knee System is a medical device manufactured by Zimmer Biomet. It received FDA 510(k) clearance on 2024-12-20 under approval number K243293. 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 2024-12-20. It is manufactured by Zimmer Biomet. The 510(k) number is K243293.

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

Zimmer® Persona® Personalized Knee System received FDA 510(k) clearance on 2024-12-20, under approval number K243293.

What company makes Zimmer® Persona® Personalized Knee System?

Zimmer® Persona® Personalized Knee System is manufactured by Zimmer Biomet.

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

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

Related Clinical Trials

Related PubMed Literature

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.