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Arthrex Compression FT Screws

Page Type
Cleared 510(K)
510(k) Number
K182361
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2018
Days to Decision
110 days
Submission Type
Summary

Arthrex Compression FT Screws

Page Type
Cleared 510(K)
510(k) Number
K182361
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2018
Days to Decision
110 days
Submission Type
Summary