Last synced on 18 April 2025 at 11:05 pm

MASTERGRAFT Contain

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