FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACCLARENT AERA Eustachian Tube Balloon Dilation System

K Number: K171761 · Decision Jan 16, 2018
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
8
Applicant Total
45
Review Days
216

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ACCLARENT AERA Eustachian Tube Balloon Dilation System
K Number
K171761
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4180
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acclarent, Inc.
Date Received
June 14, 2017
Decision Date
January 16, 2018
Product Code
PNZ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PNZ Eustachian Tube Balloon Dilation Device

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PNZ), ordered by most recent decision date.

View all

Other Clearances by Acclarent, Inc.

K Number Device Name
K253612 Acclarent AERA Eustachian Tube Balloon Dilation System
K230742 ACCLARENT AERA Eustachian Tube Dilation System
K231862 TruDi® Navigation System V3 (FG-2000-00)
K221037 TruDi Shaver Blade
K201115 Next Generation Balloon Dilation System
K201174 TruDi Curette
K193453 TruDi Probe
K190525 RELIEVA ULTIRRA Sinus Balloon Catheter
K190532 TruDi NAV Wire
K183090 Relieva Tract Balloon Dilation System
Search all 45 clearances from Acclarent, Inc. →