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ARTHREX DISTAL EXTREMITY PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111253
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2011
Days to Decision
90 days
Submission Type
Summary

ARTHREX DISTAL EXTREMITY PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111253
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2011
Days to Decision
90 days
Submission Type
Summary