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HX Device

Page Type
Cleared 510(K)
510(k) Number
K173919
510(k) Type
Traditional
Applicant
Human Extension , Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2018
Days to Decision
88 days
Submission Type
Summary

HX Device

Page Type
Cleared 510(K)
510(k) Number
K173919
510(k) Type
Traditional
Applicant
Human Extension , Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2018
Days to Decision
88 days
Submission Type
Summary