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icotec Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K233215
510(k) Type
Traditional
Applicant
Icotec AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
5/17/2024
Days to Decision
234 days
Submission Type
Summary

icotec Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K233215
510(k) Type
Traditional
Applicant
Icotec AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
5/17/2024
Days to Decision
234 days
Submission Type
Summary