Cleared Special

K142252 - XprESS Multi-Sinus Dilation Tool

K142252 is an FDA 510(k) clearance for XprESS Multi-Sinus Dilation Tool, manufactured by Entellus Medical, Inc.. The device is a Class 1 Ear, Nose, Throat device with product code LRC cleared through the Special 510(k) pathway after a 64-day FDA review.

K142252 · Entellus Medical, Inc. · Ear, Nose, Throat device
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Oct 2014
Decision
64d
Days
Class 1
Risk

K142252 is an FDA 510(k) clearance for the XprESS Multi-Sinus Dilation Tool. 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 October 17, 2014 after a review of 64 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Entellus Medical, Inc. devices

FDA 510(k) Submission Details - K142252

510(k) Number K142252 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 14, 2014
Decision Date October 17, 2014
Days to Decision 64 days
Submission Type Special
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
25d faster than avg
Panel avg: 89d · This submission: 64d
Pathway characteristics
Modification to existing cleared device.

LRC Device Classification - Class 1, General Controls

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 54
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