Cleared Traditional

K152434 - XprESS Multi-Sinus Dilation System

K152434 is the FDA 510(k) clearance for XprESS Multi-Sinus Dilation System by Entellus Medical, Inc.. It is a Class 1 Ear, Nose, Throat device (product code LRC) cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K152434 · Entellus Medical, Inc. · Ear, Nose, Throat device
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Nov 2015
Decision
85d
Days
Class 1
Risk

K152434 is an FDA 510(k) clearance for the XprESS Multi-Sinus Dilation System. Classified as Instrument, Ent Manual Surgical (product code LRC), Class I - General Controls.

Submitted by Entellus Medical, Inc. (Plymouth, US). The FDA issued a Cleared decision on November 20, 2015 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.4420 - the FDA ear, nose and throat device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Entellus Medical, Inc. devices

Submission Details

510(k) Number K152434 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 2015
Decision Date November 20, 2015
Days to Decision 85 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
4d faster than avg
Panel avg: 89d · This submission: 85d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LRC Instrument, Ent Manual Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.4420
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - LRC Instrument, Ent Manual Surgical

All 32
Devices cleared under the same product code (LRC) and FDA review panel - the closest regulatory comparables to K152434.
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RELIEVA SCOUT SINUS DILATION SYSTEM
K140160 · Acclarent, Inc. · Feb 2014