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Arthrex Intramedullary Nails

Page Type
Cleared 510(K)
510(k) Number
K230257
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2023
Days to Decision
167 days
Submission Type
Summary

Arthrex Intramedullary Nails

Page Type
Cleared 510(K)
510(k) Number
K230257
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2023
Days to Decision
167 days
Submission Type
Summary