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FortiBridge Anterior Cervical Plate System

Page Type
Cleared 510(K)
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)
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