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Renovis A200 PS Knee System as part of the Renovis A200 Knee System

Page Type
Cleared 510(K)
510(k) Number
K190122
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2019
Days to Decision
146 days
Submission Type
Summary

Renovis A200 PS Knee System as part of the Renovis A200 Knee System

Page Type
Cleared 510(K)
510(k) Number
K190122
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2019
Days to Decision
146 days
Submission Type
Summary