Persona Partial Knee
K-Number: K251834 · 2025-08-15
ApplicantZimmer Biomet
Decision Date2025-08-15
Product CodeHSX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Persona Partial Knee is a medical device manufactured by Zimmer Biomet. It received FDA 510(k) clearance on 2025-08-15 under approval number K251834. The device is classified under product code HSX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Persona Partial Knee?
Persona Partial Knee is a medical device that received FDA 510(k) clearance on 2025-08-15. It is manufactured by Zimmer Biomet. The 510(k) number is K251834.
When was Persona Partial Knee approved by the FDA?
Persona Partial Knee received FDA 510(k) clearance on 2025-08-15, under approval number K251834.
What company makes Persona Partial Knee?
Persona Partial Knee is manufactured by Zimmer Biomet.
What is the FDA product code for Persona Partial Knee?
The FDA product code for Persona Partial Knee is HSX.
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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.