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ARIX Humerus System

Page Type
Cleared 510(K)
510(k) Number
K230938
510(k) Type
Special
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/3/2023
Days to Decision
30 days
Submission Type
Summary

ARIX Humerus System

Page Type
Cleared 510(K)
510(k) Number
K230938
510(k) Type
Special
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/3/2023
Days to Decision
30 days
Submission Type
Summary