JNJ Gets FDA Nod for Dual-Energy Catheter, Boosting Electrophysiology
Johnson & Johnson (JNJ) has received U.S. FDA approval for its Dual Energy THERMOCOOL SMARTTOUCH SF Platform, a single catheter capable of delivering both radiofrequency and pulsed field energy, simplifying atrial fibrillation ablation procedures.
JNJ's Dual-Energy Catheter Gains FDA Approval
Johnson & Johnson (JNJ) has secured U.S. FDA approval for its Dual Energy THERMOCOOL SMARTTOUCH SF Platform, a novel ablation catheter for treating atrial fibrillation. The catheter allows physicians to use both radiofrequency (RF) and pulsed field (PF) energy from a single device, streamlining workflow and enhancing procedure efficiency.
The Product
The catheter represents a leap in electrophysiology, combining two energy modalities in one device and integrating with JNJ's CARTO mapping system. This integration enables precise heart mapping and catheter guidance.
Pricing and Availability
Pricing has not been disclosed. U.S. procedures are expected to begin after a phased commercial rollout this summer.
Competition
The new catheter faces competition from similar devices by Medtronic and Boston Scientific, which have also developed pulsed field ablation technologies. However, the single-catheter dual-energy design may give JNJ a competitive edge.
Potential Impact on JNJ
The approval is expected to strengthen JNJ's position in the rapidly growing atrial fibrillation treatment market. This innovation could boost its market share in electrophysiology, positively impacting its medical devices segment revenue.
Frequently Asked Questions
Found this useful? Share it