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INTERSTIM WITHOUT LIMITS™

Recharge-free and rechargeable options let you choose what’s best for each patient.

Alert Indications, Safety, and Warnings

NOT ALL BATTERIES ARE CREATED EQUAL

Head-to-head overdischarge battery testing proves Medtronic outperforms Axonics^®.^*

Learn more about the independent tests that reached this conclusion.

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OVERDRIVE^™BATTERY TECHNOLOGY

At the core of InterStim^™ Micro is Medtronic Overdrive^™battery technology, a non-traditional lithium-ion battery.

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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 scans²
Flexibility for MRI providers

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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 system next to the InterStim Micro device.

RECHARGE WITHOUT LIMITS

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

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	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.

Conducted by an independent laboratory, this battery bench testing yields data that emphasizes Medtronic Overdrive™ technology’s indisputable quality and performance over Axonics^® traditional lithium-ion batteries. This testing was designed to examine true battery behavior, beyond device level features, for robust system performance under overdischarge. The study included five InterStim™ Micro batteries and two batteries removed from new Axonics^® stimulators. Overdischarge was induced via a slow constant current discharge to 0V, followed by a one week hold at 0V. Cells were characterized by 50, 0%-100% state-of-charge cycles, as defined by their respective manufacturers’ specifications.¹

^†

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.

Medtronic data on file.

MRI guidelines for InterStim™ systems 97810 3058 3023 — Instructions for use (M980291A016 Rev A).