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Arthrex Distal Radius System

Page Type
Cleared 510(K)
510(k) Number
K143749
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2015
Days to Decision
93 days
Submission Type
Summary

Arthrex Distal Radius System

Page Type
Cleared 510(K)
510(k) Number
K143749
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2015
Days to Decision
93 days
Submission Type
Summary