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Arthrx Fracture Plates

Page Type
Cleared 510(K)
510(k) Number
K213837
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2022
Days to Decision
144 days
Submission Type
Summary

Arthrx Fracture Plates

Page Type
Cleared 510(K)
510(k) Number
K213837
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2022
Days to Decision
144 days
Submission Type
Summary