Balloon Catheter


Product Overview

Balloon Catheter
iVAS - 0705310500


Device Description

A catheter-like device with an inflatable balloon at the distal end used for the reduction of fractures and/or creation of a void in cancellous bone [e.g., in the spine for a vertebral compression fracture (VCF), hand, tibia, radius, and calcaneus]. It is commonly used for kyphoplasty, which involves its insertion into a patient's back to reduce a vertebral body fracture by compression of cancellous bone and/or movement of the endplates as the balloon is inflated. After the device is removed, orthopaedic bone cement is introduced into the created void to stabilize the vertebra. This is a single-use device.


Environmental Conditions

  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 60.00
    • 10.00
  • Storage Environment Temperature - Degrees Celsius
    • 25.00
    • 12.00

  • Device Sizes

  • Needle Gauge: 11.0 Gauge
  • Length: 10.0 Millimeter
    • Needle Gauge: 11.0 Gauge
    • Length: 10.0 Millimeter


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: NDN

    Device Name: Cement, Bone, Vertebroplasty

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: OR

    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: 888.3027

    Third Party Flag: N

    Medical Specialty: OR


    Device Identifiers

    Device Id: 37613252506004

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 07613252506003

    Package Quantity: 3

    Package Discontinue Date: 7/8/2021 12:00:00 AM

    Package Status: Not in Commercial Distribution

    Package Type: pack


    Device Id: 07613252506003

    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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