Zimmer® Persona® Personalized Knee System
K-Number: K243293 · 2024-12-20
Device Summary
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
Other Devices by Zimmer Biomet
Related Devices (Code: MBH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.