510(k) · Cleared
Recalled · Class II · 2017Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
C2 Therapeutics, Inc. · GEH Unit, Cryosurgical, Accessories
Cleared on Apr 13, 2016 as substantially equivalent to K131523 (C2 Therapeutics, 2013) and 3 other predicates after a 239-day review. Its family tree reaches back 16 generations to 1995. 6 later devices descend from it. It has been recalled once.
- Decided
- Apr 13, 2016
- Review
- 239 days
- Class
- Class II
- Product code
- GEH
- Recalls
- 1
- Predicates
- 4
Its longest line of descent runs back 16 generations to K943450 (1995). 67 ancestors in all, the oldest K790187 (1979). 6 later devices descend from it, 2 citing it directly.
- Root · 16 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 12 generations between
- 3 generations backK060169 Barrx Halo Coagulation System, Barrx Halo Coagulation Generator…Barrx Medical, Incorporated · 2006
- 2 generations backK062723 HALO90 Coagulation CatheterBarrx Medical, Incorporated · 2006
- 1 generation backK083737 Halo Ablation CatheterBarrx Medical, Incorporated · 2009
- This deviceK152329 Coldplay Cryoballoon; Focal Ablation System, Full Ablation System…C2 Therapeutics, Inc. · 2016
- Descendant · cites it directly · 5 of its ownK161202 C2 Cryoballoon Ablation SystemC2 Therapeutics, Inc. · 2017 · Recalled
- Descendant · cites it directly · 4 of its ownK163684 C2 CryoBalloon Ablation SystemC2 Therapeutics, Inc. · 2018 · Recalled
- Descendant · 2 generations on · 3 of its ownK190194 C2 CryoBalloon Catheter (Pear), C2 CryoBalloon (Standard), C2…Pentax Medical, A Division of Pentax of America, Inc. · 2019
- Descendant · 3 generations on · 2 of its ownK203024 C2 CryoBalloon Catheter (Pear), C2 CryoBalloon Catheter (Standard)…Pentax of America, Inc. · 2020
- Descendant · 4 generations on · 1 of its ownK212814 C2 CryoBalloon Ablation SystemPentax of America, Inc. · 2021
Show all 16 generations
- Root · 16 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 15 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
- 14 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
- 13 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
- 12 generations backK971532 Arthrocare Electrosurgery SystemArthrocare Corp. · 1997
- 11 generations backK013139 Stellartech Coagulation SystemStellartech Research Corp. · 2001
- 10 generations backK032062 Stellartech Coagulation System, Models (1100C-115 & 1100C-230)Stellartech Research Corp. · 2003
- 9 generations backK032452 Modification to: Stellartech Coagulation System, Models 1100C-115 &…Stellartech Research Corp. · 2003
- 8 generations backK032721 Modification to: Stellartech Coagulation System (Models 1100C-115 &…Stellartech Research Corp. · 2003
- 7 generations backK040240 Stellartech Coagulation System (Models 1100C-115 & 1100C-230)Stellartech Research Corp. · 2004
- 6 generations backK041383 Stellartech Coagulation System, Models 1100C-115 and 1100C-230Stellartech Research Corp. · 2004
- 5 generations backK042909 Stellartech Coagulation System, Models 1100C-115A & 1100C-230AStellartech Research Corp. · 2004
- 4 generations backK050831 Stellartech Coagulation System 2, Models 1100C-115A and 1100C-230AStellartech Research Corp. · 2005
- 3 generations backK060169 Barrx Halo Coagulation System, Barrx Halo Coagulation Generator…Barrx Medical, Incorporated · 2006
- 2 generations backK062723 HALO90 Coagulation CatheterBarrx Medical, Incorporated · 2006
- 1 generation backK083737 Halo Ablation CatheterBarrx Medical, Incorporated · 2009
- This deviceK152329 Coldplay Cryoballoon; Focal Ablation System, Full Ablation System…C2 Therapeutics, Inc. · 2016
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K161202C2 Cryoballoon Ablation SystemC2 Therapeutics, Inc. · 2017 · cites it directly5descendants
- K163684C2 CryoBalloon Ablation SystemC2 Therapeutics, Inc. · 2018 · cites it directly4descendants
- K190194C2 CryoBalloon Catheter (Pear), C2 CryoBalloon (Standard), C2 CryoBalloon Controller, C2…Pentax Medical, A Division of Pentax of America, Inc. · 2019 · 2 generations on3descendants
- K203024C2 CryoBalloon Catheter (Pear), C2 CryoBalloon Catheter (Standard), C2 CryoBalloon…Pentax of America, Inc. · 2020 · 3 generations on2descendants
- K212814C2 CryoBalloon Ablation SystemPentax of America, Inc. · 2021 · 4 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −16 | K943450 | Arthrocare Arthroscopic Electrosurgery System Model 970 | Arthrocare Corp. | 1995 | — |
| −15 | K961069 | Arthrocare Urologic Multi-Electrode Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −14 | K962445 | Arthrocare Dental Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −13 | K964849 | Arthrocare Dermatologic Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −12 | K971532 | Arthrocare Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −11 | K013139 | Stellartech Coagulation System | Stellartech Research Corp. | 2001 | — |
| −10 | K032062 | Stellartech Coagulation System, Models (1100C-115 & 1100C-230) | Stellartech Research Corp. | 2003 | — |
| −9 | K032452 | Modification to: Stellartech Coagulation System, Models 1100C-115 & 100C-230 | Stellartech Research Corp. | 2003 | — |
| −8 | K032721 | Modification to: Stellartech Coagulation System (Models 1100C-115 & 1100C-230) | Stellartech Research Corp. | 2003 | — |
| −7 | K040240 | Stellartech Coagulation System (Models 1100C-115 & 1100C-230) | Stellartech Research Corp. | 2004 | — |
| −6 | K041383 | Stellartech Coagulation System, Models 1100C-115 and 1100C-230 | Stellartech Research Corp. | 2004 | — |
| −5 | K042909 | Stellartech Coagulation System, Models 1100C-115A & 1100C-230A | Stellartech Research Corp. | 2004 | — |
| −4 | K050831 | Stellartech Coagulation System 2, Models 1100C-115A and 1100C-230A | Stellartech Research Corp. | 2005 | — |
| −3 | K060169 | Barrx Halo Coagulation System, Barrx Halo Coagulation Generator, Barrx… | Barrx Medical, Incorporated | 2006 | — |
| −2 | K062723 | HALO90 Coagulation Catheter | Barrx Medical, Incorporated | 2006 | — |
| −1 | K083737 | Halo Ablation Catheter | Barrx Medical, Incorporated | 2009 | — |
| 0 (this device) | K152329 | Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe… | C2 Therapeutics, Inc. | 2016 | — |
| +1 | K161202 | C2 Cryoballoon Ablation System | C2 Therapeutics, Inc. | 2017 | 1 |
| +1 | K163684 | C2 CryoBalloon Ablation System | C2 Therapeutics, Inc. | 2018 | 4 |
| +2 | K190194 | C2 CryoBalloon Catheter (Pear), C2 CryoBalloon (Standard), C2 CryoBalloon… | Pentax Medical, A Division of Pentax of America, Inc. | 2019 | — |
| +3 | K203024 | C2 CryoBalloon Catheter (Pear), C2 CryoBalloon Catheter (Standard), C2… | Pentax of America, Inc. | 2020 | — |
| +4 | K212814 | C2 CryoBalloon Ablation System | Pentax of America, Inc. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1980 | 1 | 0 |
| 1981 | 2 | 0 |
| 1984 | 2 | 0 |
| 1985 | 1 | 0 |
| 1986 | 1 | 0 |
| 1990 | 1 | 0 |
| 1992 | 1 | 0 |
| 1994 | 2 | 0 |
| 1995 | 2 | 0 |
| 1996 | 5 | 0 |
| 1997 | 5 | 0 |
| 1998 | 4 | 0 |
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2002 | 5 | 0 |
| 2004 | 1 | 0 |
| 2005 | 3 | 0 |
| 2006 | 2 | 0 |
| 2007 | 3 | 0 |
| 2010 | 2 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
| 2015 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2024 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in GEH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new GEH device
- #1 K211099 Freeze’n Clear Skin Clinic Warts & Tagsscore 25.4 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K131523 | Cryoballoon Focal Ablation SystemSummary page 4…21 CFR§878.4350(a)(2) Regulatory Class: Class II Product Code: GEH III. PREDICATE DEVICES Coldplay CryoBalloon™ Ablation System: K131523, K151054 CSA Medical truFreeze: K143625 Barrx HALO: K083737 CSA Medical has reported two design-related… | 2013 |
| * | K151054 | Coldplay Full CryoBalloon Ablation System and Coldplay Swipe CryoBalloon Ablation SystemSummary page 4…R§878.4350(a)(2) Regulatory Class: Class II Product Code: GEH III. PREDICATE DEVICES Coldplay CryoBalloon™ Ablation System: K131523, K151054 CSA Medical truFreeze: K143625 Barrx HALO: K083737 CSA Medical has reported two design-related recalls f… | 2015 |
| * | K143625 | truFreeze SystemSummary page 4…ass: Class II Product Code: GEH III. PREDICATE DEVICES Coldplay CryoBalloon™ Ablation System: K131523, K151054 CSA Medical truFreeze: K143625 Barrx HALO: K083737 CSA Medical has reported two design-related recalls for the truFreeze device. Barrx… | 2015 |
| * | K083737 | Halo Ablation CatheterSummary page 4…ct Code: GEH III. PREDICATE DEVICES Coldplay CryoBalloon™ Ablation System: K131523, K151054 CSA Medical truFreeze: K143625 Barrx HALO: K083737 CSA Medical has reported two design-related recalls for the truFreeze device. Barrx Medical has reported three d… | 2009 |
What descends from it? (6)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 6, 2017 | Class II | Z-1477-2017 | Under Investigation by firm | The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is tightened onto the controller. That could compromise the integrity and result in damage to the Controller Cap. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 21 years and passes through 4 companies; a new generation was cleared every 7 months on median.
- 6 of the 67 ancestors have a recall of any class.
- Of its descendants, K161202 (C2 Therapeutics, Inc., 2017) has gone furthest, with 5 descendants of its own.
- 2 other devices also cite its predicate K131523.
How does its category compare?
All GEH devicesGEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · GEH
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEH
77in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEH
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GEH
171in 2025
MAUDE reports naming product code GEH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 6 | 71 | 3 | 23 |
| 2008 | 1 | — | 2 | 29 |
| 2009 | 4 | 121 | 13 | 21 |
| 2010 | 4 | 86 | 4 | 173 |
| 2011 | 7 | 91 | 0 | 61 |
| 2012 | 4 | 96 | 3 | 91 |
| 2013 | 4 | 76 | 0 | 91 |
| 2014 | 6 | 42 | 2 | 57 |
| 2015 | 11 | 72 | 0 | 97 |
| 2016 | 15 | 60 | 0 | 143 |
| 2017 | 12 | 83 | 0 | 216 |
| 2018 | 6 | 42 | 1 | 208 |
| 2019 | 6 | 115 | 1 | 455 |
| 2020 | 8 | 113 | 37 | 277 |
| 2021 | 6 | 206 | 0 | 213 |
| 2022 | 6 | 56 | 0 | 230 |
| 2023 | 8 | 136 | 2 | 164 |
| 2024 | 9 | 85 | 0 | 141 |
| 2025 | 10 | 77 | 0 | 171 |
| 2026 | 8 | 148 | 2 | — |
What is it indicated for?
The Coldplay CryoBalloon™ Focal Ablation System, Coldplay CryoBalloon™ Full Ablation System, and Coldplay CryoBalloon™ Swipe Ablation System are intended for use as a cryosurgical tool in the field of general surgery, specifically for endoscopic applications, to include ablation of Barrett’s Esophagus with high grade dysplasia.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K152329 · printed Nov 6, 2026
Cite this page
510(k) Report. “K152329: Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152329
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026