Medtronic Advances in Robotic Surgery and Cardiac Treatments

Medtronic, a leading medical technology company, is making significant strides in robotic surgery and cardiac treatments, positioning itself for growth in key markets. The company's latest developments include progress on its Hugo robotic surgery system and expansion in the pulsed field ablation (PFA) and renal denervation spaces.
Hugo Robotic Surgery System Nears FDA Submission
Medtronic is on the verge of a major milestone for its Hugo robotic surgery system. CEO Geoff Martha announced that the company plans to file for U.S. market authorization with the Food and Drug Administration (FDA) by the end of March. The initial submission will focus on urology indications, with clinical trials for hernia and benign gynecology procedures already completed.
The Hugo system, which received CE mark approval for the European market in 2021, has seen significant uptake in international markets. Martha reported that Hugo procedure volume has more than doubled year over year, indicating growing adoption and utilization.
Medtronic anticipates a U.S. launch for Hugo in its fiscal year 2026, which typically begins in late April. The company expects Hugo to be a "growth driver for our surgical business in fiscal '26, and a meaningful growth driver for Medtronic in the midterm," according to Martha.
Cardiac Ablation Solutions and Renal Denervation Show Promise
Medtronic's cardiac ablation solutions business, particularly in the pulsed field ablation (PFA) space, is experiencing rapid growth. The company projects that this segment will become a $1 billion business in its fiscal 2025 year, with a clear path to $2 billion as the PFA portfolio expands.
The adoption of PFA technology for treating atrial fibrillation has been swift, with physicians embracing it over traditional radiofrequency and cryoablation methods. Medtronic, along with competitors like Boston Scientific, launched PFA products early last year, contributing to one of the fastest-growing areas in medical technology.
In the renal denervation market, Medtronic is one of only two companies with FDA-approved products. The company is anticipating Medicare coverage for renal denervation devices within the next eight months, which Martha described as a "massive" opportunity. Medtronic is proactively preparing for this by activating new accounts across the U.S. and helping healthcare providers establish Symplicity clinics and care pathways.
Martha emphasized the potential impact of renal denervation coverage, stating, "Upon coverage, this will be an immediate growth driver and will become a significant source of growth for the company."
References
- Medtronic nears FDA submission for Hugo robot
CEO Geoff Martha said Medtronic would submit its application for urological procedures to the Food and Drug Administration by the end of March.
Explore Further
What are the potential challenges Medtronic might face in obtaining FDA approval for the Hugo robotic surgery system?
What are the key differences between pulsed field ablation and traditional ablation methods in terms of efficacy and safety?
How does Medtronic's Hugo robotic surgery system compare to competitive robotic systems in the market?
What is the projected target market size for the pulsed field ablation segment by fiscal year 2025?
How might Medicare coverage for renal denervation devices impact Medtronic's financial performance and competitive standing?