K251834
- 510(k) number
- K251834
- Device name
- Persona Partial Knee
- Applicant
- Zimmer Biomet IN · US
- Product code
- HSX — Prosthesis, Knee, Femorotibial, Non-Constrained, Cem
- Decision date
- 2025-08-15
- Date received
- 2025-06-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K251834.pdf
Official FDA record: K251834
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.