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Keos Anterior Cervical Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K212450
510(k) Type
Traditional
Applicant
Keos
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2022
Days to Decision
305 days
Submission Type
Summary

Keos Anterior Cervical Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K212450
510(k) Type
Traditional
Applicant
Keos
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2022
Days to Decision
305 days
Submission Type
Summary