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ClariFix Device

Page Type
Cleared 510(K)
510(k) Number
K160669
510(k) Type
Traditional
Applicant
ARRINEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2016
Days to Decision
107 days
Submission Type
Summary

ClariFix Device

Page Type
Cleared 510(K)
510(k) Number
K160669
510(k) Type
Traditional
Applicant
ARRINEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2016
Days to Decision
107 days
Submission Type
Summary