Last synced on 25 January 2026 at 3:41 am

ROSA® Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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