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Next Generation Balloon Dilation System

Page Type
Cleared 510(K)
510(k) Number
K201115
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2020
Days to Decision
122 days
Submission Type
Summary

Next Generation Balloon Dilation System

Page Type
Cleared 510(K)
510(k) Number
K201115
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2020
Days to Decision
122 days
Submission Type
Summary