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Arthrex 2.5 mm Tenodesis Screw

Page Type
Cleared 510(K)
510(k) Number
K183395
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
131 days
Submission Type
Summary

Arthrex 2.5 mm Tenodesis Screw

Page Type
Cleared 510(K)
510(k) Number
K183395
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
131 days
Submission Type
Summary