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Arthrex DynaNite K-Wire

Page Type
Cleared 510(K)
510(k) Number
K200068
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2020
Days to Decision
168 days
Submission Type
Summary

Arthrex DynaNite K-Wire

Page Type
Cleared 510(K)
510(k) Number
K200068
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2020
Days to Decision
168 days
Submission Type
Summary