Cleared Traditional

K152329 - Coldplay Cryoballoon

Also marketed or referenced as:
Focal Ablation System, Full Ablation System Swipe Ablation System

K152329 is an FDA 510(k) clearance for Coldplay Cryoballoon, manufactured by C2 Therapeutics, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEH cleared through the Traditional 510(k) pathway after a 239-day FDA review.

K152329 · C2 Therapeutics, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2016
Decision
239d
Days
Class 2
Risk

K152329 is an FDA 510(k) clearance for the Coldplay Cryoballoon. 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 April 13, 2016 after a review of 239 days - an extended review 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all C2 Therapeutics, Inc. devices

FDA 510(k) Submission Details - K152329

510(k) Number K152329 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 2015
Decision Date April 13, 2016
Days to Decision 239 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
124d slower than avg
Panel avg: 115d · This submission: 239d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 K152329.
AtriCure cryoICE cryo-ablation probe (CRYO3), AtriCure cryoICE cryoFORM cryo-ablation probe (CRYOF)
K180137 · AtriCure, Inc. · Feb 2018
C2 CryoBalloon Ablation System
K163684 · C2 Therapeutics, Inc. · Jan 2018
IcePearl 2.1 CX L, IceForce 2.1 CX L
K162599 · Galil Medical , Ltd. · Oct 2016
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