Last synced on 14 November 2025 at 11:06 pm

XPRESS BALLOON DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102003
510(k) Type
Traditional
Applicant
Entellus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2010
Days to Decision
99 days
Submission Type
Summary

XPRESS BALLOON DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102003
510(k) Type
Traditional
Applicant
Entellus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2010
Days to Decision
99 days
Submission Type
Summary