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Relieva SpinPlus Balloon Sinuplasty System

Page Type
Cleared 510(K)
510(k) Number
K143541
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2015
Days to Decision
128 days
Submission Type
Summary

Relieva SpinPlus Balloon Sinuplasty System

Page Type
Cleared 510(K)
510(k) Number
K143541
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2015
Days to Decision
128 days
Submission Type
Summary