Stereotaxis Receives FDA Approval for MAGiC Catheter
Stereotaxis announced it obtained U.S. Food and Drug Administration approval for the MAGiC Magnetic Interventional Ablation Catheter. "FDA approval of MAGiC is a significant milestone for Stereotaxis and the community of physicians pioneering robotics in electrophysiology. It ensures the benefits of Robotic Magnetic Navigation can support patients with complex and critical heart rhythm disorders, represents a major advance in robotic cardiac ablation technology, and provides a foundation for continued technological and clinical progress. We want to thank and recognize the team members, partners, clinicians and reviewers who made this milestone possible. We look forward to seeing MAGiC serve as a key pillar in our effort to continue making robotics broadly impactful and beneficial in electrophysiologys," said David Fischel, Stereotaxis Chairman and CEO.
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Stereotaxis Receives FDA Approval for MAGiC Magnetic Ablation Catheter
- FDA Approval: Stereotaxis announced it has received FDA approval for its MAGiC Magnetic Interventional Ablation Catheter, marking a significant advancement in surgical robotics and is expected to drive market demand for cardiac ablation therapies.
- Technological Innovation: The MAGiC catheter utilizes robotic navigation and computer-controlled magnetic fields to offer levels of precision and stability often unattainable with traditional catheters, aiming to improve treatment outcomes for complex patient populations, particularly those with arrhythmias.
- Market Expansion: This catheter is specifically designed for patients with anatomical abnormalities or prior surgical interventions that limit access via conventional manual catheter navigation, which is expected to significantly enhance the accessibility of minimally invasive cardiac ablation therapies to underserved patient populations.
- Strategic Implications: The FDA approval not only enhances Stereotaxis's competitiveness in the cardiac treatment space but also has the potential to generate new revenue streams, further solidifying its leadership position in the surgical robotics market.

Stereotaxis Receives FDA Approval for MAGiC Catheter, Advancing Cardiac Treatment Technology
- FDA Approval Milestone: Stereotaxis's receipt of FDA approval for the MAGiC catheter marks a significant advancement in cardiac electrophysiology, enabling complex arrhythmia patients to benefit from robotic magnetic navigation technology, thereby enhancing the company's competitiveness in the medical device market.
- Technological Innovation: The MAGiC catheter is navigated by highly precise computer-controlled magnetic fields, offering maneuverability and stability levels often unattainable with traditional catheters, which is expected to significantly improve the safety and efficacy of cardiac ablation procedures.
- Market Potential: Designed for complex patient populations that are difficult to treat with conventional methods, the catheter is anticipated to expand Stereotaxis's market share in cardiac care, addressing the growing medical demand.
- Clinical Impact: The launch of the MAGiC catheter will not only promote the application of robotic technology in electrophysiology but also provide physicians with safer and more effective treatment options, further solidifying Stereotaxis's leadership in innovative medical technology.






