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Arthrex Low Profile Screws

Page Type
Cleared 510(K)
510(k) Number
K190921
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2019
Days to Decision
204 days
Submission Type
Summary

Arthrex Low Profile Screws

Page Type
Cleared 510(K)
510(k) Number
K190921
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2019
Days to Decision
204 days
Submission Type
Summary