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ROSA® Knee System

Page Type
Cleared 510(K)
510(k) Number
K221928
510(k) Type
Traditional
Applicant
Orthosoft D/B/A Zimmer Cas
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/4/2022
Days to Decision
95 days
Submission Type
Summary

ROSA® Knee System

Page Type
Cleared 510(K)
510(k) Number
K221928
510(k) Type
Traditional
Applicant
Orthosoft D/B/A Zimmer Cas
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/4/2022
Days to Decision
95 days
Submission Type
Summary