Last synced on 25 January 2026 at 3:41 am

KeYi Total Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230120
510(k) Type
Traditional
Applicant
Beijing Keyi Medical Device Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
458 days
Submission Type
Summary

KeYi Total Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230120
510(k) Type
Traditional
Applicant
Beijing Keyi Medical Device Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
458 days
Submission Type
Summary