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MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071942
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2007
Days to Decision
151 days
Submission Type
Summary

MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071942
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2007
Days to Decision
151 days
Submission Type
Summary