Meet InterStim X™ our newest recharge-free system for patients living with bladder and bowel control symptoms. InterStim X™ is the next generation of the first and most established Sacral Neuromodulation technology.
Discover our 30+ years of innovation in Sacral Neuromodulation
Powerful
Recharge-free neurostimulator with over a decade of battery life1 and up to 15 years under low energy settings2
Proprietary 5th generation battery chemistry manufactured exclusively by Medtronic
Detailed display on smart programmer with clearly visible information
Personalized
Seven distinct programmes and four custom options available on the smart programmer
More features and flexibility to tailor patient therapy with the smart programmer*
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
Medtronic, is one of the most trusted global leaders in healthcare technology that has been partnering with physicians since 1949. The InterStim™ Systems are the preferred choice for sacral neuromodulation therapy.
*** InterStim™ Implant Numbers, version 1.0, August-2022
HCP related
Patient related
The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s).
Please note that the intended use of a product may vary depending on geographical approvals.
See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events.
For an MRI compatible device(s), consult the MRI information in the device manual(s) before performing an MRI.
If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com.
Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.
Medtronic products placed on European markets bear the CE mark and the UKCA mark, if applicable.
For any further information, contact your local Medtronic representative and/or consult the Medtronic website at cema.medtronic.com.
References
*Compared to patient fob.
**Under certain conditions. See approved labeling for details. Patients with InterStim™ SureScan™ MRI leads only
*** InterStim™ Implant Numbers, version 1.0, August-2022
∏ Based on computational modeling and experimental data
1. Under expected therapy settings and telemetry use.
2. Please see System Eligibility, Battery Longevity, Specifications manual for battery longevity estimates.