Deep brain stimulation
Medtronic, the originator and world leader in deep brain stimulation (DBS), is boldly transforming brain modulation through sensing-enabled DBS.
Our 30-year commitment to DBS patients is deep and far-reaching.
180K+
Medtronic has served over 180 thousand patients1
70+
Countries offering DBS with dedicated support1
$400M+
Invested in R&D over past 5 years1
50+
Globally, Medtronic brain modulation is sponsoring or supporting more than 50 DBS studies across 15 countries1
Engineered to adapt
Meet the
Percept™ family.
The Percept™ family with exclusive BrainSense™ technology† empowers clinicians to adapt DBS therapy to a patients' evolving needs over time.
Empowering patient freedom with patient-first capabilities for flexibility and convenience.
Enabling personalization with data-driven insights that allow you to adapt therapy to your patients' needs.
Designed for upgradability Engineered for future software updates designed for the Percept™ platform without a neurostimulator device exchange.
Clinician
and patient
programmer
Percept™ PC and Percept™ RC neurostimulators with BrainSense™ technology†
SenSight™
directional
leads
Find
MRI resources
Medtronic MR Conditional‡ DBS systems are backed by more than 14 years of MRI research and testing history.
Access Medtronic Academy
Access on-demand DBS resources, procedural videos, webinars, and more at Medtronic Academy.
This material is for Healthcare Professionals in countries with applicable health authority product registrations.
Important: Always refer to the Instructions For Use (IFU) packaged with the product/e-IFU for complete instructions, indications, contraindications, warnings, and precautions.
† The sensing feature of the Percept™ PC system and Percept™ RC system is intended for use in patients receiving DBS where chronically recorded bioelectric data may provide useful, objective information regarding patient clinical status. The majority of patients with Parkinson’s disease have an identifiable signal. Signal may not be present or measurable in patients treated for essential tremor, dystonia*, epilepsy, or obsessive-compulsive disorder*.
* Humanitarian device: The effectiveness of these devices for the treatment of dystonia and obsessive-compulsive disorder has not been demonstrated.
‡ 
Under specific conditions. Refer to product labeling for full list of conditions: https://manuals.medtronic.com/manuals/mri/region
1
Medtronic data on file.