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Savion DLVR Guidewire, Savion FLX Guidewire

Page Type
Cleared 510(K)
510(k) Number
K180726
510(k) Type
Traditional
Applicant
Boston Scientific Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2018
Days to Decision
90 days
Submission Type
Summary

Savion DLVR Guidewire, Savion FLX Guidewire

Page Type
Cleared 510(K)
510(k) Number
K180726
510(k) Type
Traditional
Applicant
Boston Scientific Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2018
Days to Decision
90 days
Submission Type
Summary