K242543
- 510(k) number
- K242543
- Device name
- Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)
- Applicant
- Zimmer, Inc. IN · US
- Product code
- MBH — Prosthesis, Knee, Patello/Femorotibial, Semi-Constra
- Decision date
- 2024-11-22
- Date received
- 2024-08-26
- 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: K242543.pdf
Official FDA record: K242543
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.