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Medtronic Announces Comprehensive U.S. Launch of New InterStim™ Micro Neurostimulator

Key Takeaway: Medtronic has launched its FDA-approved InterStim Micro neurostimulator for sacral neuromodulation therapy in the U.S., with the first implant performed at Cleveland Clinic. This device aims to improve bladder and bowel control for patients suffering from overactive bladder (OAB) and fecal incontinence (FI). The launch is supported by extensive clinical data and aims to enhance the quality of life for millions of affected adults.

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POSITIVE FACTORS

  • FDA approval of the InterStim Micro neurostimulator enhances treatment options.
  • First patient implant at Cleveland Clinic signifies successful launch.
  • Device aims to improve quality of life for patients with OAB and FI.
  • Backed by extensive clinical data and physician collaboration.

Full Press Release Details

First Patient Receives New Sacral Neuromodulation Device Implant atCleveland Clinic
DUBLIN, Aug. 05, 2020 (GLOBE NEWSWIRE) --Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced that its recently FDA-approved InterStim™ Micro neurostimulator for sacral neuromodulation (SNM) therapy is now available in the United States. Cleveland Clinic performed the first patient implant in the nation with the new device.
Sacral neuromodulation sends electrical impulses to the sacral nerves located in the lower back to improve bladder and bowel control. Unlike oral medications that target the muscular component of bladder control, SNM offers control of symptoms through direct modulation of the nerve activity, normalizing the communication between the bladder and the brain.1,2
"Effective long-term bladder and bowel control is needed for almost 55 million adults3,4,5,6in the United States who often experience regular accidents and/or frequency issues that are associated with overactive bladder (OAB) and fecal incontinence (FI),” said Sandip Vasavada, M.D., professor at the Glickman Urological and Kidney Institute and section head Female Pelvic Medicine and Reconstructive Surgery, Cleveland Clinic. “A new FDA-approved option for these patients is a step forward.” Dr. Vasavada discloses compensation for speaker/trainer/educator activities.

About InterStim Micro

“Patients unfortunately limit their lives socially, professionally and personally due to OAB and FI,” said Howard Goldman, M.D., professor and vice chairman of Quality and Patient Safety, Glickman Urological and Kidney Institute, Cleveland Clinic. “With this newly FDA-approved device, we have a new option and can offer more patients sacral neuromodulation therapy and improve their quality of life.” Dr. Goldman discloses compensation for speaker/trainer/educator and consulting activities.
“OAB and FI patients want to live a life without limits, and we designed our new rechargeable SNM system to advance this reality,” said Brooke Story, vice president and general manager of the Pelvic Health& Gastric Therapies business, which is part of the Restorative Therapies Group at Medtronic. “We created our entire InterStim portfolio in partnership with physicians backed by a 25-year track record of experience in sacral neuromodulation including over 325,000 implanted patients, 5-year clinical data and more than 1,000 peer-reviewed articles. We are confident our InterStim systems give patients and physicians the best choice in SNM therapy.”
About MedtronicMedtronic plc (www.medtronic.com), headquartered in Dublin, Ireland, is among the world’s largest medical technology, services and solutions companies – alleviating pain, restoring health and extending life for millions of people around the world. Medtronic employs more than 90,000 people worldwide, serving physicians, hospitals and patients in more than 150 countries. The company is focused on collaborating with stakeholders around the world to take healthcare Further, Together.
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.
-end-
1Leng WW, Morrisroe SN. Sacral nerve stimulation for the overactive bladder. Urol Clin N Am. 2006;33:491-501.
2Kenefick NJ, Emmanuel A, Nicholls RJ. Effect of sacral nerve stimulation on autonomic nerve function. British Journal of Surgery. 2003;90:1256-1260.
3Stewart WF, et al. Prevalence and burden of overactive bladder in the United States. World J Urol. 2003 May;20(6):327-336.
4United Nations, Department of Economic and Social Affairs, Population Division (2011). World Population Prospects: The 2010 Revision, CD-ROM Edition.
5Whitehead WE, Borrud L, Goode PS, et al. Pelvic floor disorders network. Fecal incontinence in US adults: epidemiology and risk factors. Gastroenterology. 2009;137: 512-517
6United States Quick Facts. United States Census Bureau Web site. Available at: https://www.census.gov/quickfacts/table/ PST045215/00. Accessed July 19, 2016.
David T. YoungPublic Relations+1-774-284-2746
Ryan WeispfenningInvestor Relations+1-763-505-4626

Frequently Asked Questions

What is the InterStim Micro neurostimulator?

The InterStim Micro neurostimulator is a device for sacral neuromodulation therapy, aimed at improving bladder and bowel control.

Where was the first implant of the InterStim Micro performed?

The first implant of the InterStim Micro neurostimulator was performed at Cleveland Clinic.

What conditions does the InterStim Micro treat?

It treats overactive bladder (OAB) and fecal incontinence (FI) by modulating nerve activity.

Who developed the InterStim Micro neurostimulator?

The device was developed by Medtronic, a leader in medical technology.

Last updated: Aug 5, 2020