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Keos Anterior Cervical Interbody Fusion Device System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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