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Arthrex Small External Fixation System

Page Type
Cleared 510(K)
510(k) Number
K232897
510(k) Type
Special
Applicant
Arthrex Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2023
Days to Decision
30 days
Submission Type
Summary

Arthrex Small External Fixation System

Page Type
Cleared 510(K)
510(k) Number
K232897
510(k) Type
Special
Applicant
Arthrex Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2023
Days to Decision
30 days
Submission Type
Summary