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AXIOS Stent and Electrocautery Enhanced Delivery System

Page Type
Cleared 510(K)
510(k) Number
K203132
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2021
Days to Decision
178 days
Submission Type
Summary

AXIOS Stent and Electrocautery Enhanced Delivery System

Page Type
Cleared 510(K)
510(k) Number
K203132
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2021
Days to Decision
178 days
Submission Type
Summary