510(k) K251834

Device
Persona Partial Knee
Applicant
Zimmer Biomet
510(k) number
K251834
Product code
HSX
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-15
Date received
2025-06-16
Regulation
888.3520
Classification name
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Courtney Williams
Address
1800 W. Center St. Warsaw IN US 46580 46580

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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