K232175
- 510(k) number
- K232175
- Device name
- XN Knee Prosthesis System
- Applicant
- Beijing Chunlizhengda Medical Instruments Co., Ltd. CN
- Product code
- JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrai
- Decision date
- 2024-04-14
- Date received
- 2023-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K232175.pdf
Official FDA record: K232175
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.