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ROSA® Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213708
510(k) Type
Traditional
Applicant
Orthosoft, Inc (d/b/a Zimmer CAS)
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/22/2022
Days to Decision
149 days
Submission Type
Summary

ROSA® Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213708
510(k) Type
Traditional
Applicant
Orthosoft, Inc (d/b/a Zimmer CAS)
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/22/2022
Days to Decision
149 days
Submission Type
Summary