K243293
- 510(k) number
- K243293
- Device name
- Zimmer® Persona® Personalized Knee System
- Applicant
- Zimmer Biomet IN · US
- Product code
- MBH — Prosthesis, Knee, Patello/Femorotibial, Semi-Constra
- Decision date
- 2024-12-20
- Date received
- 2024-10-18
- 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: K243293.pdf
Official FDA record: K243293
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.