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VERTEBRON SCP CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040003
510(k) Type
Traditional
Applicant
Vertebron, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2004
Days to Decision
84 days
Submission Type
Summary

VERTEBRON SCP CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040003
510(k) Type
Traditional
Applicant
Vertebron, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2004
Days to Decision
84 days
Submission Type
Summary