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EUROPA™ Navigated Instruments

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230369
510(k) Type
Traditional
Applicant
Mirus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2023
Days to Decision
133 days
Submission Type
Summary

EUROPA™ Navigated Instruments

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230369
510(k) Type
Traditional
Applicant
Mirus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2023
Days to Decision
133 days
Submission Type
Summary