INS 37603 ACTIVA SC INLINE EXT US


Product Overview

INS 37603 ACTIVA SC INLINE EXT US
Activa® - 37603


Device Description

An assembly of sterile implantable devices designed to apply electrical stimuli to specific areas of the deep brain for the treatment of movement disorders (e.g. essential tremor, symptoms of Parkinson’s disease, epilepsy, dystonia), psychiatric disorders (e.g. obsessive-compulsive disorder, depression, anxiety disorder), and/or to treat chronic, severe, intractable pain. It typically consists of leads implanted in the brain, lead extensions, and a pulse generator that is typically implanted near the sternum.


Environmental Conditions

  • Handling Environment Temperature - Degrees Fahrenheit
    • 126.00
    • 0.00
  • Handling Environment Temperature - Degrees Celsius
    • 52.00
    • -18.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: MHY

    Device Name: Stimulator, Electrical, Implanted, For Parkinsonian Tremor

    Device Class: 3

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 2

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: MFR

    Device Name: Stimulator, Brain, Implanted, For Behavior Modification

    Device Class: f

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 6

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: MRU

    Device Name: Implanted Subcortical Electrical Stimulator (Motor Disorders)

    Device Class: f

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 6

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: OLM

    Device Name: Deep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)

    Device Class: f

    Physical State: Electrodes, extension and IPG

    Definition: The device is indicated for bilateral stimulation of the anterior limb of the internal capsule, this device is indicated as an adjunct to medications and as an alternative to anterior capsulotomy for treatment of chronic, severe, treatment-resistant Obsessive Compulsive Disorder (OCD) in adult patients who have failed at least three Selective Serotonin Reuptake Inhibitors (SSRIs).

    Submission Type ID: 6

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Deep brain stimulation

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: Anterior limb of the internal capsule in the brain

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: NHL

    Device Name: Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

    Device Class: 3

    Physical State: N/A

    Definition: Bilateral stimulation of the internal globus pallidus (GPi) or the subthalamic nucleus (STN) using Medtronic Activa Parkinson's Control Therapy is indicated for adjunctive therapy in reducing some of the symptoms of advanced, levodopa-responsive Parkinsons disease that are not adequately controlled with medication.

    Submission Type ID: 2

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Device Identifiers

    Device Id: 00613994761071

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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