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CETRA Anterior Cervical Plate System

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