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INTERSTIM WITHOUT LIMITS™

Recharge-free and rechargeable options let you choose what’s best for each patient.
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Alert Indications, Safety, and Warnings

THERAPY WITHOUT LIMITS

We continue to advance sacral neuromodulation by offering updated full-body MRI labeling.* We have improved:

  • Patient access to MRI exams
  • Wait times between scans1
  • Flexibility for MRI providers

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THE BEST CHOICE KEEPS GETTING BETTER

New and improved MRI labeling for the InterStim™ systems with Surescan™ MRI leads.

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Test WITHOUT LIMITS

The InterStim™ basic evaluation allows patients to explore the therapy before making a long-term decision. Test with the best and expect actionable results within a week.

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The InterStim II device next to the smartphone patient programmer.

RELIEF WITHOUT LIMITS

The recharge-free InterStim™ II system may be the best choice for most people because it’s simple, convenient, and low maintenance.

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The InterStim II device next to the smartphone patient programmer.

RECHARGE   WITHOUT LIMITS  

The InterStim™ Micro system is the smallest sacral neuromodulation device on the market.

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The InterStim system next to the InterStim Micro device.
InterStim™ II System InterStim™ Micro System

MRI SCANS

Allows full-body scans*

Allows full-body scans*

BATTERY

Recharge-free

Rechargeable Overdrive™ battery technology

BATTERY LIFE

Approximately 5-6 years†

At least 15 years

DEVICE SIZE

12.5 cm3

2.8 cm3

ROUTINE MAINTENANCE

None

Weekly recharging of 20 minutes‡

COMPONENTS/ACCESSORIES

Smart programmer, communicator

Smart programmer, communicator, recharger, charging dock, recharging belt

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PATIENT SELECTION

Learn more about which patients are indicated for bladder control and bowel control therapy.

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BUILDING THE FUTURE TOGETHER 

Medtronic provides the innovative technology, expert support, and specialized services your practice needs to thrive.

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The most common adverse events experienced include pain at implant sites, new pain, lead migration, infection, technical or device problems, adverse change in bowel or voiding function, and undesirable stimulation or sensations. Any of these may require additional surgery or cause return of symptoms.

Complications can occur with the evaluation, including tissue damage, infection, and technical problems with the device. Patients should be instructed on operating the programmer and given precautions related to the evaluation.

*

Under certain conditions. See approved labeling for details. Patients with InterStim™ SureScan™ MRI leads only.

†

Battery life may vary based on therapy settings.

‡

Under standard therapy settings and appropriate recharger placement.

1

MRI Guidelines for InterStim™ systems 97810 3058 3023 – Instructions for use (M980291A016 Rev A)