Last synced on 14 November 2025 at 11:06 pm

MASTERGRAFT Contain

Page Type
Cleared 510(K)
510(k) Number
K151172
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2015
Days to Decision
105 days
Submission Type
Summary

MASTERGRAFT Contain

Page Type
Cleared 510(K)
510(k) Number
K151172
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2015
Days to Decision
105 days
Submission Type
Summary