Last synced on 14 November 2025 at 11:06 pm

TRIBRID® Unicompartmental Knee System

Page Type
Cleared 510(K)
510(k) Number
K232114
510(k) Type
Traditional
Applicant
Kyocera Medical Technologies Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2024
Days to Decision
265 days
Submission Type
Summary

TRIBRID® Unicompartmental Knee System

Page Type
Cleared 510(K)
510(k) Number
K232114
510(k) Type
Traditional
Applicant
Kyocera Medical Technologies Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2024
Days to Decision
265 days
Submission Type
Summary