The Company’s nsPFA™ System demonstrates the ability to provide cardiac ablation and mapping capabilities with a single catheter in preclinical studies
The Company collaborated with CardioNXT to integrate its iMap System with the nsPFA System to demonstrate the benefits of an integrated 3D Mapping, Navigation and nsPFA System
The poster highlights the integration of Pulse Bioscience’s nsPFA System with CardioNXT’s iMAP 3-D mapping and navigation system. The preclinical study demonstrated the integrated system’s ability to navigate the catheter for accurate ablation and to create pre and post-ablation voltage maps.
“We are excited to announce our work and collaborative efforts with CardioNXT and these highly respected physicians to develop a new and exciting modality for cardiac ablation and the treatment of arrhythmias,” said
Novel Nanosecond Pulsed Field Ablation Compatible with 3D Mapping & Navigation System presented
About Pulsed Field Ablation
Pulsed field ablation is an exciting new modality for ablating tissue and in particular cardiac tissue for the treatment of cardiac arrhythmias. Current treatment options, including existing PFA systems, utilize pulse durations in the microseconds, stimulating skeletal muscle resulting in patient spasm. As such, deeper sedation and paralytics may be needed during these procedures. To combat this dynamic
All statements in this press release that are not historical are forward-looking statements, including, among other things, statements relating to Pulse Biosciences’ expectations concerning its collaboration with CardioNXT, such as whether an integrated product using a mapping catheter and Pulse Biosciences’ nsPFA System can accurately ablate cardiac cells and create post-ablation voltage maps, statements concerning customer adoption and future use of the CellFX System to address a range of conditions such as atrial fibrillation, statements relating to the effectiveness of the Company’s nsPFA technology and the CellFX System to non-thermally clear cells while sparing adjacent non-cellular tissue, and Pulse Biosciences’ expectations, whether stated or implied, regarding whether the Company’s nsPFA technology will become a disruptive treatment option for treating cardiac arrhythmias and whether future clinical studies will show the CellFX System is safe and effective to treat atrial fibrillation or any other medical condition, and other future events. These statements are not historical facts but rather are based on Pulse Biosciences’ current expectations, estimates, and projections regarding Pulse Biosciences’ business, operations and other similar or related factors. Words such as “may,” “will,” “could,” “would,” “should,” “anticipate,” “predict,” “potential,” “continue,” “expects,” “intends,” “plans,” “projects,” “believes,” “estimates,” and other similar or related expressions are used to identify these forward-looking statements, although not all forward-looking statements contain these words. You should not place undue reliance on forward-looking statements because they involve known and unknown risks, uncertainties, and assumptions that are difficult or impossible to predict and, in some cases, beyond Pulse Biosciences’ control. Actual results may differ materially from those in the forward-looking statements as a result of a number of factors, including those described in Pulse Biosciences’ filings with the