IceCure Medical’s ProSense Cryoablation System Receives the US FDA Marketing Authorization for Breast Cancer

IceCure Medical’s ProSense Cryoablation System Receives the US FDA Marketing Authorization for Breast Cancer


Shots:

  • The US FDA granted De Novo marketing authorization to ProSense cryoablation system for treating women (≥70yrs.) with biologically low-risk breast tumors (≤1.5cm) on adjuvant endocrine therapy
  • ProSense is a minimally invasive cryosurgical tool that uses liquid nitrogen to freeze & destroy tumors in breast, kidney, lung & liver, with similar safety & efficacy observed in the ICE3 trial for low-risk breast cancer compared to lumpectomy
  • Additionally, FDA requested IceCure to conduct a post-market surveillance study of ~400 pts across 30 sites, which will also serve as commercial centers offering ProSense cryoablation to eligible breast cancer pts

Ref: PRNewsWire | Image: IceCure Medical| Press Release

Related News:- Hologic Secures the US FDA’s 510(k) Clearance & European CE Mark for Panther Fusion GI Bacterial Assays to Advance Gastroenteritis Diagnostics

PharmaShots! Your go-to media platform for customized news ranging for multiple indications. For more information connect with us at connect@pharmashots.com



Source link

Leave a Reply

Your email address will not be published. Required fields are marked *