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ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K220115
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2022
Days to Decision
119 days
Submission Type
Summary

ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K220115
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2022
Days to Decision
119 days
Submission Type
Summary