Cleared Special

K180138 - AtriCure cryoICE cryo-ablation probe (C...

K180138 is the FDA 510(k) clearance for AtriCure cryoICE cryo-ablation probe (C... by AtriCure, Inc.. It is a Class 2 Neurology device (product code GXH) cleared through the Special 510(k) pathway after a 29-day FDA review.

K180138 · AtriCure, Inc. · Neurology device
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Feb 2018
Decision
29d
Days
Class 2
Risk

K180138 is an FDA 510(k) clearance for the AtriCure cryoICE cryo-ablation probe (CRYO2). Classified as Device, Surgical, Cryogenic (product code GXH), Class II - Special Controls.

Submitted by AtriCure, Inc. (Mason, US). The FDA issued a Cleared decision on February 15, 2018 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4250 - the FDA neurology 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 AtriCure, Inc. devices

Submission Details

510(k) Number K180138 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 17, 2018
Decision Date February 15, 2018
Days to Decision 29 days
Submission Type Special
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 148d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code GXH Device, Surgical, Cryogenic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4250
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Neurology devices follow this clearance model.

Regulatory Peers - GXH Device, Surgical, Cryogenic

All 10
Devices cleared under the same product code (GXH) and FDA review panel - the closest regulatory comparables to K180138.
AtriCure cryoICE cryo-ablation probe (Cryo2), AAtriCure cryoICE cryoSPHERE cryoablation probe (CryoS, CryoS-L)
K200697 · AtriCure, Inc. · Dec 2020
AtriCure cryoICE cryoSPHERE cryoablation probe
K182565 · AtriCure, Inc. · Nov 2018
iovera system
K173763 · Myoscience, Inc. · Feb 2018
Atricure Cryo Module System
K142203 · AtriCure, Inc. · Nov 2014