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Arthrex Mesh Plates

Page Type
Cleared 510(K)
510(k) Number
K201677
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2020
Days to Decision
75 days
Submission Type
Summary

Arthrex Mesh Plates

Page Type
Cleared 510(K)
510(k) Number
K201677
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2020
Days to Decision
75 days
Submission Type
Summary