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dynaMX Intramedullary Implant

Page Type
Cleared 510(K)
510(k) Number
K170326
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2017
Days to Decision
168 days
Submission Type
Summary

dynaMX Intramedullary Implant

Page Type
Cleared 510(K)
510(k) Number
K170326
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2017
Days to Decision
168 days
Submission Type
Summary