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VERTEX(r) Reconstruction System

Page Type
Cleared 510(K)
510(k) Number
K152338
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2015
Days to Decision
70 days
Submission Type
Summary

VERTEX(r) Reconstruction System

Page Type
Cleared 510(K)
510(k) Number
K152338
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2015
Days to Decision
70 days
Submission Type
Summary