C2 Therapeutics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
C2 Therapeutics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Redwood, Ca, US.
Historical record: 7 cleared submissions from 2015 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by C2 Therapeutics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - C2 Therapeutics, Inc.
7 devices
Cleared
Jan 23, 2018
C2 CryoBalloon Ablation System
General & Plastic Surgery
391d
Cleared
Jan 05, 2017
C2 Cryoballoon Ablation System
General & Plastic Surgery
252d
Cleared
May 19, 2016
C2 CryoBalloon Focal Pear Catheter
General & Plastic Surgery
41d
Cleared
Apr 13, 2016
Coldplay Cryoballoon
General & Plastic Surgery
239d
Cleared
Jan 07, 2016
Coldplay CryoBalloon® Ablation System
General & Plastic Surgery
28d
Cleared
Oct 13, 2015
Boa Endoscopic Valve
Gastroenterology & Urology
71d
Cleared
Jul 07, 2015
Coldplay Full CryoBalloon Ablation System and Coldplay Swipe CryoBalloon...
General & Plastic Surgery
78d