Class Class II
Persona Partial Knee (K251834)
Description
Persona Partial Knee by Zimmer Biomet, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251834
Clearance Date2025-08-15
Clearance TypeTraditional
Product CodeHSX
Regulation Number888.3520
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251834
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Persona Partial Knee (K251834) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K161592 | Persona Partial Knee System | Biomet, Inc. | 2016 |
Trace the full predicate network for K251834
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.