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ARIX Ankle Distal Tibia System

Page Type
Cleared 510(K)
510(k) Number
K170313
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/27/2017
Days to Decision
176 days
Submission Type
Summary

ARIX Ankle Distal Tibia System

Page Type
Cleared 510(K)
510(k) Number
K170313
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/27/2017
Days to Decision
176 days
Submission Type
Summary