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Arthrex Low Profile Screws

Page Type
Cleared 510(K)
510(k) Number
K203239
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2020
Days to Decision
57 days
Submission Type
Summary

Arthrex Low Profile Screws

Page Type
Cleared 510(K)
510(k) Number
K203239
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2020
Days to Decision
57 days
Submission Type
Summary