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MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation

Page Type
Cleared 510(K)
510(k) Number
K232154
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2023
Days to Decision
53 days
Submission Type
Summary

MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation

Page Type
Cleared 510(K)
510(k) Number
K232154
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2023
Days to Decision
53 days
Submission Type
Summary