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ARTHREX HUMERAL FRACTURE PLATES AND SCREWS

Page Type
Cleared 510(K)
510(k) Number
K041965
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2004
Days to Decision
49 days
Submission Type
Summary

ARTHREX HUMERAL FRACTURE PLATES AND SCREWS

Page Type
Cleared 510(K)
510(k) Number
K041965
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2004
Days to Decision
49 days
Submission Type
Summary