InterStim XTM system Recharge-free neurostimulator for bowel and bladder control
The next generation of the first and most trusted sacral neuromodulation system.1,2,3
Download the brochure
Overview
Powerful
- Recharge-free neurostimulator with over a decade of battery life4 and up to 15 years under low energy settings5
- Proprietary 5th generation battery chemistry manufactured exclusively by Medtronic
- Detailed display on smart programmer with clearly visible information
Personalised
- Seven distinct programmes and four custom options available on the smart programmer
- More features and flexibility to tailor patient therapy with the smart programmer*
Sacral Neuromodulation
30 years of innovation
Have more options with InterStim™ systems
SureScan™ MRI technology
Enables patients with an InterStim X™ or InterStim™ Micro system to get full-body† 1.5T and 3T MRI scans.
- No impedance checks required prior to MRI scans
- Scans allowed even if patients have had out-of-range impedances
- MRI mode is easy to activate or deactivate on the smart programmer without clinician or Medtronic interaction
- Digital display for clear confirmation of MRI mode activation
InterStim™ Smart programmer
- Benefit from a single programming device across both recharge-free and rechargeable devices
- Offers tailored patient therapy with a choice of up to 11 programs
- Empowers patients to manage their therapy easily at home or on the go
InterStim™ basic evaluation
- Allows patients to explore the therapy before making a long-term decision
- Trust our basic evaluation lead advanced coil technology that is designed to minimize electrode movement during daily activities‡
Clinical and patient support
Gives you confidence working with a company that offers:
- Expert technical and field-based suport
- Decades of experience
- Patient support services
90+
clinical
trials
400,000+
patients
treated§
30+
years SNM
experience
1,000+
Clinical
articles
The most common adverse events experienced during clinical studies 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.
Model specifications
|
Model |
97800 |
|---|---|
|
Battery type |
Recharge-free |
|
Weight |
22 g |
|
Height |
44 mm |
|
Length |
51 mm |
|
System components |
|
Additional resources
MRI
Eligibility
Get the details on specific MRI compatibilty for neuromodulation therapies.
Product
manuals
Follow us on
LinkedIn
Follow Medtronic Pelvic Health on LinkedIn for the latest updates on our products and therapies.
*
Compared to patient fob.
†
Under certain conditions. See approved labeling for details. Patients with InterStim™ SureScan™ MRI leads only
‡
Based on computational modeling and experimental data
§
Number of InterStim Implant Numbers, version 2.0, July-2023
1
Siegel S, Noblett K, Mangel J, et al. Five-year follow-up results of a prospective, multicenter study of patients with overactive bladder treated with sacral neuromodulation. The Journal of Urology 2018, 229 -236.
2
Medtronic InterStim Therapy Clinical Summary (2018).
3
Hull T, Giese C, Wexner SD, et al. Long-term durability of sacral nerve stimulation therapy for chronic fecal incontinence. Dis Colon Rectum. 2013;56(2):23.
4
Under expected therapy settings and telemetry use.
5
Please see System Eligibility, Battery Longevity, Specifications manual for battery longevity estimates.
See the device manual for detailed information regarding the instructions for use, indications, contraindications, warnings, precautions, and potential adverse events. If using an MRI SureScan® device, see the MRI SureScan® technical manual before performing an MRI. For further information, contact your local Medtronic representative and/or consult the Medtronic website at medtronic.eu website
For applicable products, consult instructions for use on www.medtronic.com/manuals.
Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser. CE0123