Cleared Special

K153541 - Coldplay CryoBalloon Ablation System

K153541 is an FDA 510(k) clearance for Coldplay CryoBalloon Ablation System, manufactured by C2 Therapeutics, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEH cleared through the Special 510(k) pathway after a 28-day FDA review.

K153541 · C2 Therapeutics, Inc. · General & Plastic Surgery device
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Jan 2016
Decision
28d
Days
Class 2
Risk

K153541 is an FDA 510(k) clearance for the Coldplay CryoBalloon® Ablation System. Classified as Unit, Cryosurgical, Accessories (product code GEH), Class II - Special Controls.

Submitted by C2 Therapeutics, Inc. (Redwood, Ca, US). The FDA issued a Cleared decision on January 7, 2016 after a review of 28 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4350 - the FDA general and plastic surgery 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 C2 Therapeutics, Inc. devices

FDA 510(k) Submission Details - K153541

510(k) Number K153541 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 2015
Decision Date January 07, 2016
Days to Decision 28 days
Submission Type Special
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 115d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

GEH Device Classification - Class 2, Special Controls

Product Code GEH Unit, Cryosurgical, Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4350
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GEH Unit, Cryosurgical, Accessories

All 129
Devices cleared under the same product code (GEH) and FDA review panel - the closest regulatory comparables to K153541.
C2 CryoBalloon Ablation System
K163684 · C2 Therapeutics, Inc. · Jan 2018
IcePearl 2.1 CX L, IceForce 2.1 CX L
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cryoFORM cryoICE cryoablation probe
K152337 · AtriCure, Inc. · Mar 2016
IcePearl 2.1 CX Cryoablation Needle, IcePearl 2.1 CX Prostate Cryoablation Kit Visual-ICE System, IceFORCE 2.1 CX Cryoablation Needle, IceFORCE 2.1 CX Prostate Cryoablation Kit Visual-ICE System
K152133 · Galil Medical , Ltd. · Aug 2015
ERBECRYO 2 Cryosurgical Unit with accessories
K151041 · Erbe USA, Inc. · May 2015
cryoICE croablation probe
K142441 · AtriCure, Inc. · Oct 2014