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ARTHREX FRACTURE PLATES

Page Type
Cleared 510(K)
510(k) Number
K123241
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2013
Days to Decision
170 days
Submission Type
Summary

ARTHREX FRACTURE PLATES

Page Type
Cleared 510(K)
510(k) Number
K123241
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2013
Days to Decision
170 days
Submission Type
Summary