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RIGEL 3DR Anterior Cervical Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K200685
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2020
Days to Decision
87 days
Submission Type
Summary

RIGEL 3DR Anterior Cervical Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K200685
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2020
Days to Decision
87 days
Submission Type
Summary