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FortiBridge 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
K162250
510(k) Type
Special
Applicant
NANOVIS SPINE LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2016
Days to Decision
77 days
Submission Type
Summary

FortiBridge 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
K162250
510(k) Type
Special
Applicant
NANOVIS SPINE LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2016
Days to Decision
77 days
Submission Type
Summary