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icotec Anterior Cervical Plate System

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