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The Percept™ family

Percept RC PC CP PP

Designed for the needs of today and tomorrow, the Percept™ family is:

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 and engineered to allow for future software updates for the Percept™ platform without a neurostimulator device exchange


DBS Percept™ family video

Percept™ PC neurostimulator

Percept

The recharge-free model blends ergonomic design with cutting-edge battery technology.
 

Ergonomic design Percept™ PC neurostimulator is designed for comfort, with the thinnest PC on the market†,1-3.
Designed to last The Percept™ PC device has a projected mean longevity >5 years for median energy-user and features smart battery technology offering real-time estimation of battery longevity§, to keep keep your patients informed.
Designed to adapt BrainSense™ technologyΩ and advanced programming capabilities let you personalize therapy to your patients’ evolving needs over time.
Broad indication coverage Indicated for: PD, ET, epilepsy, dystonia*, OCD*

† As compared to Competitor 1. MP92328632-05 REV-A. As compared to Competitor 2. IPG. ARTEN600150429 - B.
‡ For median energy use in DBS for patients with Parkinson’s disease.
§ Based on current actual battery level and therapy settings from last seven days.
*Humanitarian device: The effectiveness of these devices for the treatment of dystonia has not been demonstrated.

Percept™ RC neurostimulator

Percept RC product image showcasing from the front and side view

Meet the newest member of the Percept™ family. Percept™ RC offers patients a rechargeable version specifically designed to be:

Small Patient comfort
The smallest, thinnest, dual-channel DBS device available††.
Smart Rapid recharging
Patients can charge under normal conditions (from 10% to 90% full) in less than an hour‡‡.

Greater than 99% capacity at 15 years with weekly recharge, it is designed to offer a more consistent recharge experience over time.
Adaptive Designed to adapt
BrainSense™ technologyΩ and advanced programming capabilities let you personalize therapy to your patients’ evolving needs over time.
Broad indication coverage Indicated for: PD, ET, epilepsy, dystonia*.

†† As compared to Competitor 1. MP92328632-05 REV-A. As compared to Competitor 2. ARTEN600150429 - B.
‡‡ For implant depths of up to 2.0cm.
*Humanitarian device: The effectiveness of these devices for the treatment of dystonia has not been demonstrated.

  

 

BrainSense technology allows you to adapt to patient needs over time with data-driven insights

Percept™ family with exclusive BrainSense™ technology

  • Uses local field potentials (LFPs) as a signal of interest that can be tracked with responses to deep brain stimulation (DBS) therapy and medications

  • Offers data-driven insights into the patient’s condition enabling clinicians to adapt DBS to a patient’s needs

  • Engineered for future software updates that allow patients to have access to additional features without a device exchange

BrainSense™ technology offers decision-making support to select and optimize programming configurations and maximize therapeutic results over time.

Screen & phone

A vast majority of patients with Parkinson’s disease have a detectable signal (LFP).4

92%
have a detectable signal in an “off-medication” state4

87%
of brain hemispheres have a detectable signal in an “on-medication” state4

15+ years
of research has informed BrainSense™ technology


Medtronic MRI advantage§§.
Always on.

Your DBS patient may need an MRI

MRI icon

~10M
scans in the U.S. performed annually5

Dr icon

77%
MRI scans ordered globally are not brain-related.6

Shaking hands icon

1 in 8
women will develop breast cancer7

 

Full-body MRI access§§

  • Medtronic offers greater freedom and scan access with 3T scans and best-in-class 1.5T MRI scan labeling8-10 for directional leads.
  • Even when having an MRI, Medtronic DBS is the only DBS system that doesn't keep a patient from receiving the care they need.8-10
  • No restrictions on prone position for breast scans with Medtronic DBS systems10

Ω 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*, or epilepsy.

*Humanitarian device: The effectiveness of these devices for the treatment of dystonia has not been demonstrated.

§§ MR Safety Triangle Under specific conditions. Refer to product labeling for full list of conditions: manuals.medtronic.com/manuals/mri/region

1

Competitor 2’s IPG Clinician’s Manual ARTEN600149416 A - (US Version), accessed on 01/02/24

2

Percept™ PC B35200 Neurostimulator with BrainSense™ Technology—Implant Manual M982261A015 REV A—Medtronic

3

Competitor 1’s Surgical Implant Manual. MP92328632-05 REV A, accessed 01/02/24

4

Darcy N, Lofredi R, Al-Fatly B, et al. Spectral and spatial distribution of subthalamic beta peak activity in Parkinson’s disease patients. Experimental Neurology. 2022:114150.

5

Information for patients. International Society for Magnetic Resonance in Medicine. https://www.ismrm.org/resources/information-for-patients. Accessed December 19, 2023.

6

BCC Publishing Staff. Medical Magnetic Resonance Imaging (MRI): Technologies and Global Markets, Report Code HLC078E. BCC Research. 2021. Available at: www.bccresearch.com/market-research/healthcare/medical-magnetic-resonance-imaging-mri-technologies-and-global-markets-report.html. Accessed December 19, 2023.

7

Key Statistics for Breast Cancer. American Cancer Society Website. www.cancer.org/cancer/breast-cancer/about/how-common-is-breast-cancer.html.​ Updated January 12, 2023. Accessed December 19, 2023

8

MRI guidelines for Competitor 1’s deep brain stimulation systems — 92195369-01, accessed on 01/02/2024

9

MRI procedure information(opens new window) for Competitor 2’s MR Conditional deep brain stimulation systems — ARTEN600090482 A, accessed on 01/02/2024.

10

MRI guidelines for Medtronic deep brain stimulation systems 37601 37602 37603 37612 B35200 B35300 — M929535A_a_092 https://manuals.medtronic.com/manuals/mri/region