BOLT X0207095 7.5x25 SHORT POST TI


Product Overview

BOLT X0207095 7.5x25 SHORT POST TI
CD HORIZON® Spinal System - X0207095


Device Description

An implantable device designed to replace one or more vertebral body(s) that has collapsed or been surgically removed due to trauma, tumour or degenerative disease. Also known as a corpectomy or vertebrectomy spacer, it is in the form of a one-piece or modular hollow cylinder made of inorganic materials (e.g., metal, polymer). It is typically used with supplemental spinal fixation and/or bone graft, and some types are adjustable for in situ adjustment of prosthesis height to allow intraoperative distraction of adjacent vertebrae.


Environmental Conditions

No Data Available


Device Sizes

  • Length: 25.0 Millimeter
  • Outer Diameter: 7.5 Millimeter
    • Length: 25.0 Millimeter
    • Outer Diameter: 7.5 Millimeter


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: True

    Sterilization Methods:

  • Moist Heat or Steam Sterilization
    • Moist Heat or Steam Sterilization


    Product Codes

    Code: MNH

    Device Name: Orthosis, Spondylolisthesis Spinal Fixation

    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: 888.3070

    Third Party Flag: N

    Medical Specialty: OR


    Code: NKB

    Device Name: Thoracolumbosacral Pedicle Screw System

    Device Class: 2

    Physical State: N/A

    Definition: Intended to provide immobilization and stabilization of spinal segments in thoracic, lumbar, and sacral spine as an adjunct to fusion.

    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: 888.3070

    Third Party Flag: N

    Medical Specialty: OR


    Code: KWQ

    Device Name: Appliance, Fixation, Spinal Intervertebral Body

    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: 888.3060

    Third Party Flag: N

    Medical Specialty: OR


    Code: MNI

    Device Name: Orthosis, Spinal Pedicle Fixation

    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: 888.3070

    Third Party Flag: N

    Medical Specialty: OR


    Code: KWP

    Device Name: Appliance, Fixation, Spinal Interlaminal

    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: 888.3050

    Third Party Flag: N

    Medical Specialty: OR


    Device Identifiers

    Device Id: 00613994304742

    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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