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VERTEX(r) Reconstruction System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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