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VERTEX™ Reconstruction System

Page Type
Cleared 510(K)
510(k) Number
K180851
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2018
Days to Decision
16 days
Submission Type
Summary

VERTEX™ Reconstruction System

Page Type
Cleared 510(K)
510(k) Number
K180851
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2018
Days to Decision
16 days
Submission Type
Summary