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Arzzt Distal Radius and Ulna System

Page Type
Cleared 510(K)
510(k) Number
K182650
510(k) Type
Traditional
Applicant
Truemed Group LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2019
Days to Decision
259 days
Submission Type
Summary

Arzzt Distal Radius and Ulna System

Page Type
Cleared 510(K)
510(k) Number
K182650
510(k) Type
Traditional
Applicant
Truemed Group LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2019
Days to Decision
259 days
Submission Type
Summary