Last synced on 25 January 2026 at 3:41 am

OptiVu ROSA MxR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220733
510(k) Type
Traditional
Applicant
Orthosoft Inc (D/B/A Zimmer Cas)
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/29/2022
Days to Decision
137 days
Submission Type
Summary

OptiVu ROSA MxR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220733
510(k) Type
Traditional
Applicant
Orthosoft Inc (D/B/A Zimmer Cas)
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/29/2022
Days to Decision
137 days
Submission Type
Summary