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OptiVu™ ROSA® MxR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230567
510(k) Type
Traditional
Applicant
Orthosoft Inc. (d/b/a Zimmer CAS)
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/13/2023
Days to Decision
104 days
Submission Type
Summary

OptiVu™ ROSA® MxR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230567
510(k) Type
Traditional
Applicant
Orthosoft Inc. (d/b/a Zimmer CAS)
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/13/2023
Days to Decision
104 days
Submission Type
Summary