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Relieva SpinPlus Nav Balloon Sinuplasty System

Page Type
Cleared 510(K)
510(k) Number
K171687
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2017
Days to Decision
90 days
Submission Type
Summary

Relieva SpinPlus Nav Balloon Sinuplasty System

Page Type
Cleared 510(K)
510(k) Number
K171687
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2017
Days to Decision
90 days
Submission Type
Summary