K243724
- 510(k) number
- K243724
- Device name
- Persona® Revision Knee System (Persona Revision SoluTion Femoral Components)
- Applicant
- Zimmer, Inc. IN · US
- Product code
- JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrai
- Decision date
- 2025-03-06
- Date received
- 2024-12-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K243724.pdf
Official FDA record: K243724
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.