Imricor Medical Systems, Inc. (ASX: IMR) is making significant progress with its NorthStar 3D Mapping System. The company has submitted the system for CE Mark approval in Europe, paving the way for its commercial launch. Imricor is also accelerating the 510(k) submission process for FDA approval in the U.S. The NorthStar system is crucial for various interventional MRI procedures, including cardiac ablations.
Imricor Medical Systems is focusing on advancing its NorthStar 3D Mapping System, targeting both European and U.S. markets. By prioritizing the NorthStar system's approval over consumable tools, Imricor is positioning itself to meet the high demand from hospitals, not just for cardiac ablations but also for broader interventional MRI applications. The company's efforts are marked by the approval to conduct the first-ever MRI-guided VT ablation in Amsterdam. Imricor's collaboration with leading MRI vendors and its strategic regulatory submissions highlight its commitment to transforming interventional procedures through MRI technology, aiming for safer and more effective treatments.
The submission of the NorthStar 3D Mapping System for CE Mark approval represents a pivotal step in our strategy to revolutionize interventional MRI procedures. We are excited to meet the demand from hospitals in Europe and the U.S., which will allow us to expand our technological footprint across these critical markets.