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Durepair Dura Regeneration Matrix

Page Type
Cleared 510(K)
510(k) Number
K161370
510(k) Type
Traditional
Applicant
Medtronic Neurosurgery
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
169 days
Submission Type
Summary

Durepair Dura Regeneration Matrix

Page Type
Cleared 510(K)
510(k) Number
K161370
510(k) Type
Traditional
Applicant
Medtronic Neurosurgery
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
169 days
Submission Type
Summary