Last synced on 2 December 2022 at 11:04 pm

XPRESS MULTI-SINUS DILATION TOOL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132440
510(k) Type
Special
Applicant
Entellus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2013
Days to Decision
59 days
Submission Type
Summary

XPRESS MULTI-SINUS DILATION TOOL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132440
510(k) Type
Special
Applicant
Entellus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2013
Days to Decision
59 days
Submission Type
Summary