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ROSA® Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230243
510(k) Type
Traditional
Applicant
Orthosoft D/B/A Zimmer Cas
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/29/2023
Days to Decision
58 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
K230243
510(k) Type
Traditional
Applicant
Orthosoft D/B/A Zimmer Cas
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/29/2023
Days to Decision
58 days
Submission Type
Summary