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Arthrex Fracture System

Page Type
Cleared 510(K)
510(k) Number
K143139
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2015
Days to Decision
74 days
Submission Type
Summary

Arthrex Fracture System

Page Type
Cleared 510(K)
510(k) Number
K143139
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2015
Days to Decision
74 days
Submission Type
Summary