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ARTHREX FRACTURE PLATES AND SCREWS

Page Type
Cleared 510(K)
510(k) Number
K141478
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2014
Days to Decision
34 days
Submission Type
Summary

ARTHREX FRACTURE PLATES AND SCREWS

Page Type
Cleared 510(K)
510(k) Number
K141478
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2014
Days to Decision
34 days
Submission Type
Summary