Geoff Martha
Chairman & Chief Executive Officer at Medtronic
Hello everyone, and thank you for joining us today.
We delivered a strong finish to the fiscal year with broad strength across our businesses. Each of our four segments delivered mid single-digit or higher revenue growth, and this was on top of a strong mid single-digit performance last year. Throughout fiscal '24, we delivered consistent mid single-digit revenue growth with over 5% for the full year. At the same time, we're making progress on our commitment to restore our earnings power, which is evident in our fiscal '25 guidance. We're executing COGS cost-out programs while maintaining pricing and maximizing efficiencies in our operating overhead. And we're translating our earnings into strong and improving cash flow, which we're investing to drive future growth and return to our shareholders.
We also continue to enhance our operating model to make the company even more resilient, and our global workforce is embracing a performance-driven culture that is translating into durable results. We made solid progress in fiscal '24, and the momentum we're building into the new year has me very excited for '25. We're at the beginning stages of new product cycles. The runway from the differentiated technologies we've recently launched, along with the innovation we will launch over the next 12 months give me significant confidence in our ability to drive durable growth. These launches put us in a strong position in some of MedTech's most attractive markets like AFib, structural heart, robotics, neuromodulation, hypertension and diabetes. And this is further enhanced as we apply AI across our portfolio.
All that to say, we are very optimistic about what we can achieve here in fiscal '25 and beyond.
Now let's turn to the details of our Q4 results where we had a number of standout performances. We look at our businesses in three categories: established market leaders, synergistic and highest growth. Our established market leader and synergistic businesses both grew mid single digits, while our highest growth businesses delivered high single-digit growth.
Looking first at our established market leaders, combined, they made up just under half of our revenue and grew 5%. The highlight of the quarter was Cranial & Spinal Technologies. After growing 6% or higher every quarter this year, CST accelerated to 9% growth in Q4. I want to say that one more time, 9% growth in Q4. This was driven by an outstanding quarter for capital sales, with neurosurgery growing 14%. We had double-digit revenue growth in Mazor robotics, StealthStation navigation, O-arm imaging and Midas Rex powered surgical instruments. And this pulled through spine implants and biologics with high single-digit growth in biologics and mid single-digit growth in core spine, including 8% core spine growth in the U.S.
We also continue to see strong adoption of unit-adapted spine intelligence, our integrated AI surgical planning solution. Here we're taking data and building deep learning models that see patterns and create personalized outcomes for patients. As I've been sharing for several quarters now, our strategy of combining best-in-class implants and biologics with our best-in-class enabling technology and then adding our unique intelligence into the procedure is a winning formula in spine. We call it the AiBLE ecosystem and it's a big competitive differentiator for us. AiBLE is creating value for patients, it's winning over surgeons all around the world, and it's changing the competitive dynamics of the spine marketplace, and it's attracting the best reps to Medtronic to expand our business.
Next in Cardiac Rhythm Management, Cardiac Pacing Therapies delivered another strong quarter of high single-digit growth. Our Micra leadless pacemaker franchise grew over 20%, driven by the adoption of our latest generation Micra AV2 and VR2, which improve procedure efficiency and increase battery longevity by 40% to 16 or 17 years. Now, we hold the vast majority of share in the leadless pacing space. We also continue to expand our pacing leadership as the only company to offer an approved lead for an innovative alternative form of pacing called conduction system pacing. Our 3830 conduction system pacing lead grew over 40%. In Defibrillation Solutions, we're seeing good early adoption of our innovative Aurora EV-ICD, which requires no leads in the heart. Now, as more implanters complete their training, we expect EV-ICD sales to ramp and become a significant driver of CRM growth, taking share from the competitor's S-ICD system.
Next in Surgical, we grew 5%. Our advanced energy product lines grew high single digits on the continued launch of our LigaSure XP Maryland Vessel Sealer. We've now taken energy share from our main competitor for six quarters in a row. Our wound management business also grew high single digits as strong sales of our V-Loc Barbed Sutures also resulted in continued share gains from our main competitor.
In Q4, we expanded the capabilities of our Touch Surgery digital ecosystem. Just as our AiBLE ecosystem is transforming spine, Touch Surgery is transforming laparoscopic and robotic surgical procedures. We collect robust data sets from surgeries, including video, to create models that inject intelligence into these procedures. We've launched 14 new AI-based algorithms on our Touch Surgery Performance Insights platform just at SAGES last month. These first-in-class algorithms automatically analyze surgical procedures from anatomy to critical structures, enabling surgeons to objectively assess performance. We also launched Touch Surgery Livestream, which enables secure and seamless telepresence, including training and proctoring from a procedure room to really anywhere in the world. Overall, adoption of our Touch Surgery ecosystem is accelerating and it's becoming a very important differentiator for our surgical franchise.
Now turning to our synergistic businesses. Combined, they grew 5% in Q4. Cardiac surgery, ENT and endoscopy all grew high single digits. Pelvic health, coronary, peripheral vascular and neuromodulation all grew mid single digits. In neuromod, brain modulation had an outstanding quarter, growing low double digits. This was the first quarter of benefit from the launch of Percept RC with BrainSense technology, the only complete sensing-enabled DBS system on the market. Here we are seeing strong uptake and excitement for this exclusive technology and it's extending our number 1 leadership position in DBS in both Europe and in the U.S.
Our neuromod business also received really great news at the end of Q4 with the U.S. FDA approving the Inceptiv closed-loop spinal cord stimulator. The Inceptiv platform is a game changer in chronic pain therapy. The device automatically senses and adjusts stimulation 50 times a second, 24/7 with no required interaction from the patient, and the therapy is delivered from the smallest and thinnest closed-loop SCS device on the market, along with the best 3T and 1.5T full body conditional MRI access. Given all these advantages will now be carried in the bags of our very large SCS sales force, we expect Pain Stim to grow above market in the coming quarters.
Now, let's cover the highlights from the businesses in our highest growth markets. Combined, they made up 20% of revenue and grew high single digits and we expect that their contribution to overall growth will accelerate over the coming quarters as we launch new technology.
I'll start this quarter with Cardiac Ablation Solutions which delivered 21% sequential growth in the quarter, including 23% in the U.S. This is driven by our pulsed field ablation products, which are more than offsetting declines in our cryo product line. Q4 marked the first quarter of our PulseSelect PFA catheter launch. It's off to a great start with strong adoption from both focal RF and single shot users. As we expand the PulseSelect launch, we also continue to advance our robust pipeline of PFA technology.
Last week, U.S. pivotal data for our Sphere-9 focal catheter were presented at HRS and published in Nature Medicine. These data were impressive, especially when you consider we were studying persistent AF patients, the most challenging to treat. We showed Sphere-9 has an excellent safety profile, superior efficiency and numerically higher freedom from recurrent AFib compared head to head with the market-leading traditional RF ablation technology.
Sphere-9 can perform both PF and RF ablation as well as high density mapping, all from a single device, and we're looking forward to offering U.S. clinicians this first of its kind wide focal catheter. The output of all this is that we expect our CAS business to continue to accelerate its growth throughout the coming fiscal year as we increase our PFA account training and catheter production to meet the high demand. And over time, we expect our CAS business will reach market growth and then win share. And this will be driven by our PFA launches and the pull-through of our broader portfolio treating the growing population of patients with AFib.
Next in Structural Heart, TAVR continues to be a very important growth driver for Medtronic and we grew high single digits in the quarter. Structural Heart had two meaningful developments during Q4. First, data from our SMART trial was published in the New England Journal of Medicine and presented at ACC last month. SMART, it clearly showed our valve was better than Edwards SAPIEN in small annulus patients who are primarily women. This is a large segment of the TAVR space, about 40%, which is larger than most realize. Now, while it takes time to broadly change clinical practice and change customer contracting, we're seeing early signs from many loyal SAPIEN users that they expect to increase their usage of Medtronic valves, and we're building our business for that growth.
The second important development in Q4 was receiving U.S. FDA approval for Evolut FX+, our newest TAVR valve. FX+ has large windows in the frame to allow easy coronary access while providing the same exceptional valve performance of our Evolut platform. We have just started the limited launch now and are receiving really strong positive feedback from physicians. Full market release is expected in August.
So when you consider our four-year low-risk data, our SMART data and our new FX+ valve, we expect this combination to drive our TAVR growth at or above the market, especially as the FX+ launch ramps in our second fiscal quarter.
Turning to Robotic Surgical Technologies, we're establishing a strong foundation here and we continue to expand the Hugo system installed base. In the U.S., we are nearing completion of our urology pivotal trial. We also have now started enrollment in two new indication studies: hernia and gynecology. In addition, our development teams are making progress bringing our advanced surgical technologies to Hugo such as ICG, and our LigaSure vessel sealing technology.
In Diabetes, our team delivered another strong quarter, growing 11% globally. In the U.S., we grew 12% as the rollout of the MiniMed 780G system continues. New U.S. users doubled year-over-year again this quarter, and since launch, we've seen a significant increase in CGM attachment rates, resulting in high-teens growth in U.S. CGM revenue in Q4. Users are choosing our differentiated 780G system for the outcomes it delivers, all with less effort and less burden. 780G is the only AID system that provides both basal insulin adjustments and correction doses every five minutes. It offers flexible glucose targets as low as 100 and features our proprietary meal detection technology. This all leads to 780G users achieving a high time and range, as well as spending more time in automation with our SmartGuard technology.
In Europe, we began the limited launch of Simplera Sync with 780G and we're preparing for a commercial launch this summer. The early users and their healthcare providers are giving us fantastic feedback. Simplera Sync is half the size of our current sensor, is disposable, and it's a lot easier to put on. And in the U.S., I'm pleased to announce that we have now submitted Simplera Sync to the FDA.
Look, the turnaround in diabetes is palpable and now becoming a sustained growth story. We're committed to getting the business back to market leadership. This is why we're investing heavily in expanding indications for 780G system and developing next generation differentiated technology. This includes durable pumps, smart pens, patch pumps, CGM and software and algorithms. You've seen us execute a steady drumbeat of submissions, product approvals and expanded indications, and this is a cadence we expect to continue. We're the only company building out a complete ecosystem of leading technology for patients who require intensive insulin management. We believe this strategy positions us well and will drive our growth as the market continues to shift to automated insulin delivery and smart dosing.
Finally turning to Hypertension, we believe Symplicity will become an important growth driver for Medtronic. Since gaining approval last year, we've been training physicians and we're getting very favorable feedback from both clinicians and patients. We've also been working very closely with both CMS and private payers in the United States and expect to make significant progress on coverage and payment here in fiscal '25. With over 1 billion people worldwide living with hypertension and every 1% penetration into the target market is over $1 billion of revenue, our Symplicity procedure represents a massive opportunity.
Now with that, lets go to Karen for a deeper look at Q4 financial performance and our fiscal '25 guidance. Karen, over to you.