Medtronic Receives FDA Approval for Expanded MRI Labeling of InterStim™ SureScan™ MRI Leads

Rhea-AI Summary

Medtronic (NYSE:MDT) announced FDA approval for expanded MRI labeling of its InterStim™ II and InterStim™ Micro sacral neuromodulation systems using SureScan™ MRI leads. This updated labeling enhances MRI scan parameters and reduces wait times, improving patient access. New features include increased B1+rms settings for MRI scans and reduced maximum duration scan wait times from 60 to 5 minutes. The SureScan technology eliminates impedance checks before MRI, streamlining patient care. Medtronic continues to innovate in SNM therapy, highlighting over 70 FDA approvals for its InterStim portfolio.

Positive

• FDA approval enhances MRI scanning options for InterStim systems.
• Increased B1+rms settings improve MRI scan consistency.
• Decreased wait time for maximum duration scans from 60 minutes to 5 minutes.
• SureScan technology eliminates impedance checks, improving efficiency.

Negative

• None.

DUBLIN, Feb. 18, 2021 /PRNewswire/ -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced it has received approval from the United States Food and Drug Administration (FDA) for expanded MRI labeling of its InterStim™ II and InterStim™ Micro sacral neuromodulation (SNM) systems that use SureScan™ MRI leads. The updated MRI Guidelines allow for a wider range of MRI scan parameters and shorter wait time between MRI scans, thereby improving patient access to MRI exams and adding flexibility for MRI providers. It applies to existing and future implants of InterStim systems that use SureScan MRI leads.

"I'm pleased to see medical technology for SNM patients continue to improve," said Howard Goldman, M.D., professor and vice chairman of Quality and Patient Safety, Glickman Urological and Kidney Institute, Cleveland Clinic. "Optimal MRI labeling is an important enabler of greater access to therapy for patients and alleviates burdens on clinicians' practices."

The revised MRI labeling provides more options to patients and physicians than the labeling of the other SNM system on the market:

• For MRI scanning facilities with B1+rms technology — the gold standard in MRI scanning technology — the new SureScan MRI lead scanning parameters¹ increases B1+rms for 1.5 Tesla scans from 3.0 µT to 4.0 µT, and 3 Tesla scans from 1.3 µT to 2.0µT. B1+rms is the gold standard because it is consistent if a patient has multiple MRI scans across different facilities.² The competitor's MRI labeling does not specify parameters for 1.5T scans with B1+rms technology.
• The new Medtronic scanning parameters¹ increases SAR limits for 1.5 Tesla scans from 0.5 W/kg to 2.0 W/kg; and for 3 Tesla scans from 0.5 W/kg to 1.4 W/kg.
• The new labeling also decreases wait time from 60 minutes to 5 minutes for maximum duration scans (30 minutes).

These guideline updates are in addition to the benefit already provided by SureScan MRI technology that impedance checks prior to an MRI scan are not required, providing more efficiency in patient care versus the other SNM system on the market.

"Our updated InterStim SureScan MRI labeling means the best choice in SNM therapy keeps getting better," said Brooke Story, president, Pelvic Health & Gastric Therapies, which is reported as part of the Restorative Therapies Group at Medtronic. "We have had over 70 FDA approvals for the InterStim portfolio and are committed to continuing to innovate so we can help physicians bring life-enhancing technologies to more patients."

About InterStim SureScan MRI Technology
SureScan MRI technology is a known and trusted brand by MRI technicians. Built on more than 19 years of full-body MRI research, 10 million simulated patient scans, and more than 1.2 million unique scanning scenarios, Medtronic SureScan MRI systems prioritize patient safety.³

About Sacral Neuromodulation
Sacral neuromodulation (SNM) uses a small device to send 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.^4,5

More than 37 million adults in the United States — almost one in six — suffer from overactive bladder (OAB),^6,7 and nearly 20 million Americans — about one in 12 — have bowel incontinence.^8,9 Many OAB sufferers limit their lives socially, professionally, and personally.¹⁰ However, as many as 45% who suffer from OAB symptoms do not seek treatment and as many as seven in 10 stop using OAB medications within six months due to intolerable side effects or unsatisfying results.^11-13

About Medtronic
Medtronic 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.

1. For the inferior to C7 vertebra.
2. Reference Manual for Magnetic Resonance Safety, Implants and Devices: 2020 Edition, Frank G. Shellock, PhD
3. Medtronic data on file.
4. Leng WW, Morrisroe SN. Sacral nerve stimulation for the overactive bladder. Urol Clin N Am. 2006;33:491-501.
5. Kenefick NJ, Emmanuel A, Nicholls RJ. Effect of sacral nerve stimulation on autonomic nerve function. British Journal of Surgery. 2003;90:1256-1260.
6. Stewart WF, et al. Prevalence and burden of overactive bladder in the United States. World J Urol. 2003 May;20(6):327-336.
7. United Nations, Department of Economic and Social Affairs, Population Division (2011). World Population Prospects: The 2010 Revision, CD-ROM Edition.
8. Whitehead 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.
9. United States Quick Facts. United States Census Bureau Web site. Available at: https://www.census.gov/quickfacts/table/ PST045215/00. Accessed July 19, 2016.
10. Dmochowski RR, Newman DK. Impact of overactive bladder on women in the United States: results of a national survey. Current Medical Research and Opinion. 2007;23:65-76.
11. Leede Research, "Views on OAB: A Study for the National Association of Continence." December 16, 2015.
12. Yu YF, Nichol MB, Yu AP, et al. Persistence and adherence of medications for chronic overactive bladder/urinary incontinence in the California Medicaid Program. Value in Health. 2005;8(4)495-505.
13. Yeaw J, Benner JS, Walt JG, Sian S, Smith DB, et al. J Manag Care Pharm. 2009;15(9):728-740.

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SOURCE Medtronic plc

FAQ

What FDA approval did Medtronic receive on February 18, 2021, for MDT?

Medtronic received FDA approval for expanded MRI labeling of its InterStim™ II and InterStim™ Micro sacral neuromodulation systems using SureScan™ MRI leads.

How does the new MRI labeling benefit patients using MDT's InterStim systems?

The new labeling allows for a wider range of MRI scan parameters and shorter wait times, improving patient access to MRI exams.

What are the new B1+rms settings for MDT's MRI scans?

New settings increase B1+rms for 1.5 Tesla scans from 3.0 µT to 4.0 µT and for 3 Tesla scans from 1.3 µT to 2.0 µT.

What efficiency advantages does SureScan technology provide for MDT's InterStim systems?

SureScan technology eliminates the need for impedance checks before MRI scans, streamlining patient care.

How many FDA approvals has Medtronic achieved for the InterStim portfolio?

Medtronic has achieved over 70 FDA approvals for its InterStim portfolio.