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Arthrex Mesh Plate System

Page Type
Cleared 510(K)
510(k) Number
K170547
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2017
Days to Decision
189 days
Submission Type
Summary

Arthrex Mesh Plate System

Page Type
Cleared 510(K)
510(k) Number
K170547
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2017
Days to Decision
189 days
Submission Type
Summary