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Medtronic Receives Category I CPT® Code Approvals for Altaviva™ and Symplicity Spyral™ Systems

The permanent codes can support physician payment, but do not determine coverage or reimbursement.

(Neutral)

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Medtronic (MDT) received American Medical Association approval for Category I procedure codes covering its Altaviva and Symplicity Spyral systems.

The permanent Current Procedural Terminology (CPT) codes replace existing Category III codes effective January 2028. Altaviva treats urge urinary incontinence and received FDA approval in September 2025 for patients who failed or could not tolerate more conservative treatments. Symplicity Spyral treats uncontrolled hypertension; its Medicare coverage was finalized in October 2025. Category I codes can support physician payment and inform commercial payer coverage decisions, but do not determine coverage, reimbursement, clinical superiority or patient access.

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3 points · 0 major

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Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.

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Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 2 points

Hollow bars mark forward-looking points. How the balance works

Positive

  • Moderate pointCategory I CPT code approvals establish permanent procedure codes for Altaviva and Symplicity Spyral.
  • Minor pointAltaviva FDA approval in September 2025 covers urge urinary incontinence after failed or intolerable conservative treatments.
  • Minor pointSymplicity Spyral Medicare coverage was finalized in October 2025.

Negative

  • Minor point. Forward-looking: it has not happened yet and may not happen.January 2028 effectiveness means the newly approved codes do not replace Category III codes immediately.
  • Minor pointCoding approvals do not determine coverage, reimbursement, clinical superiority or patient access.

Key Figures

Technologies receiving code approvals: 2 technologies Code effective date: January 2028 Clinical program enrollment: More than 5,000 patients +1 more
Technologies receiving code approvals
2 technologies
Altaviva and Symplicity Spyral
Code effective date
January 2028
New Category I CPT codes replace existing Category III codes
Clinical program enrollment
More than 5,000 patients
Medtronic SPYRAL HTN global clinical program
Patient experience
Over 40,000 patients globally
Renal denervation experience; includes Symplicity Flex and Symplicity Spyral

Key Terms

cpt, renal denervation, neuromodulation
3 terms
cpt regulatory
"approved new Category I Current Procedural Terminology (CPT®) codes"
CPT stands for Current Procedural Terminology, a standardized set of codes used to describe medical procedures and services for billing and insurance purposes. For investors, CPT codes determine how and whether healthcare providers get paid for treatments, affecting revenue streams and reimbursement risk; think of them like product barcodes that decide price and payment for clinical services. Changes to codes or coverage policies can directly alter a healthcare company's cash flow and profitability.
renal denervation medical
"Symplicity Spyral™ renal denervation (RDN) system"
Renal denervation is a minimally invasive medical procedure that reduces high blood pressure by disrupting overactive nerves around the kidneys, effectively turning down the signals that cause blood vessels to constrict. It matters to investors because clinical results, regulatory approvals, adoption by doctors and insurers, and device sales determine the size and timing of a potential new market for medical device makers and healthcare providers, similar to how a popular new tool can reshape demand in an industry.
neuromodulation medical
"Altaviva™ implantable tibial neuromodulation device"
Neuromodulation is the use of devices or targeted treatments to change how nerves or brain circuits send signals, much like adjusting the volume or tuning on an audio system to alter what you hear. For investors, it matters because these therapies can treat chronic conditions (pain, movement disorders, depression) where existing medicines fall short, creating potential markets, regulatory milestones, and durable revenue streams if technologies prove safe and effective.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Coding approvals reflect growing clinical evidence and physician adoption of Medtronic solutions addressing urge urinary incontinence and hypertension 

GALWAY, Ireland, Oct. 1, 2026 /PRNewswire/ -- Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced that the American Medical Association (AMA) approved new Category I Current Procedural Terminology (CPT®) codes for two of its technologies, which represent important long-term growth opportunities for Medtronic: Altaviva™ implantable tibial neuromodulation device for the treatment of urge urinary incontinence and Symplicity Spyral™ renal denervation (RDN) system for the treatment of uncontrolled hypertension. The new codes, which will replace existing Category III codes, are effective January 2028.

Category I CPT® codes are permanent codes assigned to procedures the AMA has determined are well established, widely performed by physicians across the United States (U.S.), and supported by robust clinical evidence, in addition to other criteria identified in the application process. While a Category I CPT® code establishes a permanent code and can help support physician payment and inform commercial payer coverage decisions, it does not determine coverage, reimbursement, clinical superiority, or patient access.

"These Category I approvals reflect the robust clinical evidence and physician adoption for innovative solutions addressing critical gaps in care and unmet patient needs," said Lindsay Bockstedt, vice president of health economics, policy, and reimbursement at Medtronic. "The decision by AMA represents meaningful progress in the reimbursement pathway for these technologies, as Medtronic remains committed to reducing barriers to broader adoption and patient access. We're grateful to the stakeholders and clinical community whose work made this possible."

The AMA approved new Category I CPT® codes applicable to procedures associated with the following Medtronic technologies:

Altaviva™ Implantable Tibial Neuromodulation Device
The Altaviva™ device was approved by the U.S. Food and Drug Administration (FDA) in September 2025, for the treatment of urge urinary incontinence (UUI) – a condition that impacts 16 million adults in the U.S. 1 The Altaviva™ device is indicated for treatment of UUI in patients who failed or could not tolerate more conservative treatments. The device is approximately half the length of a stick of chewing gum and is placed under the skin near the ankle in a minimally invasive procedure.2 The device delivers stimulation to the tibial nerve to help restore communication between the bladder and brain to improve bladder leakage symptoms. 3-4 Unlike some other treatment options, the Altaviva™ device does not require imaging for implantation and only needs local anesthesia, and it can be activated the same day as the procedure. The system is designed to provide patients with a simple, long-lasting treatment experience, including an expected 15 years of therapy under expected therapy settings. The Altaviva™ device is also MRI-compatible from the start5, offering patients peace of mind for future medical imaging needs.

Symplicity Spyral™ Renal Denervation System
The Symplicity Spyral renal denervation (RDN) system, finalized for Medicare coverage in October 2025, is an innovative, minimally invasive procedure that delivers radiofrequency energy to nerves near the kidneys that can become overactive and contribute to high blood pressure. After sedation, the doctor inserts a single thin tube (known as a catheter) into the artery leading to the kidney. Once the tube is in place, the doctor administers energy to the system to calm the excessive activity of the nerves connected to the kidney. The tube is removed, leaving no implant behind. The Medtronic SPYRAL HTN global clinical program is the most comprehensive clinical program studying RDN in more than 5,000 patients in the presence and absence of medication, and with high baseline cardiovascular risk, and is backed by experience in over 40,000 patients globally.6-13 

About Medtronic
Bold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Galway, Ireland, is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people across more than 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic, visit www.Medtronic.com and follow Medtronic on LinkedIn.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

CPT® codes, descriptions and other data only are copyright 2025 American Medical Association. All Rights Reserved. Applicable FARS/HHSARS apply.

  1. Coyne KS, Wein A, Nicholson S, Kvasz M, Chen CI, Milsom I. Economic burden of urgency urinary incontinence in the United States: a systematic review. J Manag Care Pharm. 2014
  2. Cameron AP, Chung DE, Dielubanza EJ et al. The AUA/SUFU guideline on the diagnosis and treatment of idiopathic overactive bladder (2024). J Urol. 2024;212:11-20.  
  3. Li X, Li X, Liao L. Mechanism of action of tibial nerve stimulation in the treatment of lower urinary tract dysfunction. Neuromod. 2023;27:256-266.
  4. Bhide AA, Tailor V, Fernando R, Vik K, Digesu GA. Posterior tibial nerve stimulation for overactive bladder - techniques and efficacy. Int Urogynecol J. 2020;31:865–70.
  5. M028929C001 RevC - Clinician Therapy and Programming Guide Altaviva™ Model P7850N
  6. Medtronic data on file, RDN Catheter Historical Data, Feb 2025. Data includes both Symplicity Flex and Symplicity Spyral.
  7. Kandzari DE, Townsend RR, Kario K, et al. Safety and Efficacy of Renal Denervation in Patients Taking Antihypertensive Medications. J Am Coll Cardiol. 2023 Nov 7;82(19):1809-1823.
  8. Böhm M, Kario K, Kandzari DE, et al. Efficacy of catheter-based renal denervation in the absence of antihypertensive medications (SPYRAL HTN-OFF MED Pivotal): a multicentre, randomised, sham-controlled trial. Lancet. 2020 May 2;395(10234):1444-1451. 
  9. Kario K, Ogawa H, Okumura K, et al. SYMPLICITY HTN-Japan - first randomized controlled trial of catheter-based renal denervation in asian patients -. Circ J. 2015;79(6):1222–1229.
  10. Bhatt DL, Kandzari DE, O'Neill WW, et al. A controlled trial renal denervation for resistant hypertension. N Engl J Med. April 10, 2014;370(15):1393–1401.
  11. Townsend RR, Mahfoud F, Kandzari DE, et al. Catheter-based renal denervation in patients with uncontrolled hypertension in the absence of antihypertensive medications (SPYRAL HTN-OFFMED): a randomised, sham-controlled, proof-of-concept trial. Lancet. November 11, 2017;390(10108):2160–2170.
  12. Krum H, Schlaich MP, Sobotka PA, et al. Percutaneous renal denervation in patients with treatment-resistant hypertension: final 3-year report of the Symplicity HTN-1 study. Lancet. 2014;383(9917):622–629.
  13. Medtronic data on file, RDN Catheter Historical Data, September 2026. Data includes both Symplicity Flex and Symplicity Spyral.

Contacts:


Justin Paquette

Ingrid Goldberg

Public Relations

Investor Relations

+1- 612-271-7935

+1-763-505-2696

 

 

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

When do Medtronic's Altaviva and Symplicity Spyral Category I CPT codes take effect?

The new Category I CPT codes take effect in January 2028, replacing existing Category III codes. The American Medical Association approved codes applicable to procedures associated with both systems.

Do Medtronic's new Category I CPT codes guarantee insurance coverage or reimbursement?

The new codes do not determine coverage or reimbursement. They establish permanent procedure codes that can help support physician payment and inform commercial payer coverage decisions, but also do not determine clinical superiority or patient access.

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