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Arthrex RetroFusion Screw

Page Type
Cleared 510(K)
510(k) Number
K151078
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2015
Days to Decision
23 days
Submission Type
Summary

Arthrex RetroFusion Screw

Page Type
Cleared 510(K)
510(k) Number
K151078
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2015
Days to Decision
23 days
Submission Type
Summary