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CETRA Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K162638
510(k) Type
Traditional
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2016
Days to Decision
85 days
Submission Type
Summary

CETRA Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K162638
510(k) Type
Traditional
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2016
Days to Decision
85 days
Submission Type
Summary