The POLARx cryoablation system features a POLARx FIT cryoablation balloon catheter with the ability to enable two balloon sizes. Credit: Boston Scientific Corporation or its affiliates.

The US Food and Drug Administration (FDA) has granted approval for Boston Scientific’s cryoablation system, dubbed POLARx.

The system is intended for treating paroxysmal atrial fibrillation (AF) patients.

Go deeper with GlobalData

Premium Insights

The gold standard of business intelligence.

Find out more

Related Company Profiles

View all

It features the POLARx FIT cryoablation balloon catheter built with the ability to enable two balloon sizes, 28mm and 31mm, in a single catheter.

A minimally invasive procedure, cryoablation facilitates AF treatment by delivering cryotherapy to the pulmonary vein through a balloon catheter.

This approach freezes the affected tissue to create scarring, thereby hindering irregular electrical signals.

See Also:

The new POLARx FIT catheter can be adjusted to fit the anatomy of patients during the procedure and helps address various limitations.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

According to findings from the FROZEN-AF IDE clinical trial, POLARx was found to be safe and effective in treating paroxysmal AF patients. 

At 12 months, the primary event-free rate was reported to be 96%, without any cases of persistent phrenic nerve palsy or oesophagal fistulas and moderate or severe pulmonary vein stenosis. 

Boston Scientific electrophysiology president Nick Spadea-Anello said: “The US approval of the POLARx cryoablation system, which has been used in more than 25,000 patients worldwide to date, marks an exciting advancement for the treatment of AF and a new era of cryoablation capabilities.

“By prioritising procedural flexibility and individualised care, this offering transforms a key therapy in the electrophysiology space, addresses the unmet needs of physicians and affirms our commitment to making meaningful innovations to established technologies.”

The company recently posted GAAP net income attributable to its common stockholders of $261m in Q2 2023.