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Arthrex DynaNite Nitinol Staple

Page Type
Cleared 510(K)
510(k) Number
K172052
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2017
Days to Decision
160 days
Submission Type
Summary

Arthrex DynaNite Nitinol Staple

Page Type
Cleared 510(K)
510(k) Number
K172052
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2017
Days to Decision
160 days
Submission Type
Summary