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DuraFuse Clip and Applier System

Page Type
Cleared 510(K)
510(k) Number
K213813
510(k) Type
Traditional
Applicant
Neuramedica, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
227 days
Submission Type
Summary

DuraFuse Clip and Applier System

Page Type
Cleared 510(K)
510(k) Number
K213813
510(k) Type
Traditional
Applicant
Neuramedica, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
227 days
Submission Type
Summary