the webinar

First Inceptiv™ SCS patient cases in Europe. 

Recorded on 25 January 2024

A great opportunity to understand the impact Inceptiv™ with closed-loop technology might bring to your patients therapy experience.
Faculty share their first experiences in Europe, including patients with conventional stimulation as well as modern waveform therapies, followed by the latest clinical evidence highlights.

Experts panel

Ashis Gulve round portrait
Dr. Ashish Gulve,
Dirk Rasche round portrait
Dr. Dirk Rasche,
UKSH, Germany
Isaac Pena round portrait
Dr. Isaac Peña,
HUVR, Spain
Francesco Riillo round portrait
Francesco Riillo,
Medtronic, Sr Scientist

Webinar extracts:

Dr. Gulve experience of first 15 patients implanted with Inceptiv™ SCS with closed-loop technology at 4 weeks follow-up.

Dr. Gulve DPN patient case study.

Dr. Rasche FNSS patient case study with cervical lead placement.

Dr. Peña PSPS2 Patient case study.

Get in touch to talk about Inceptiv™ SCS
and closed-loop technology


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Learn more about Inceptiv™ SCS and closed-loop technology

§Under specific conditions. Refer to product labeling for full list of conditions. All the answers assume that other eligibility requirements have been met.


Fishman M, Cordner H, Justiz R, et al.  12-Month Results from Multicenter, Open-Label, Randomized Controlled Clinical Trial Comparing Differential Target Multiplexed Spinal Cord Stimulation and Traditional Spinal Cord Stimulation in Subjects with Chronic Intractable Back Pain and Leg Pain. Pain Pract. 2021; 21: 912– 923. doi:10.1111/papr.13066


Inceptiv IFU with MRI labeling. 2023. M010773C001 Rev B. M009826C001 Rev B. M939858A028 Rev A.


Evoke SCS System User Manual. 2022 Saluda Medical. CLINUMAN-002426 Revision: 16.00.


ECHO MAC Final Clinical Study Report V1.0 2021-08-18


Medtronic Stimulation RC Clinician A71400 Programmer Application Programming Guide for Neurostimulation Systems for pain therapy. 2022. M009826C001 Rev A


Inceptiv IFU Implant manual. January 2023. M010773C002 Rev A.


Battery Performance Report D00810906 (Battery Life, Fade) - 29-Aug- 2022 Version A

See the device manual for detailed information regarding the instructions for use, the implant procedure, 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 CE0123