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Vertu® & Vertu® Ti-Bond and Crystal® & Crystal® Ti-Bond Cervical Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153352
510(k) Type
Traditional
Applicant
Spinal Elements Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2016
Days to Decision
255 days
Submission Type
Summary

Vertu® & Vertu® Ti-Bond and Crystal® & Crystal® Ti-Bond Cervical Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153352
510(k) Type
Traditional
Applicant
Spinal Elements Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2016
Days to Decision
255 days
Submission Type
Summary