DBM A42110 2.5CMX5CM FLEXGRAFTON


Product Overview

DBM A42110 2.5CMX5CM FLEXGRAFTON
GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) - A42110


Device Description

An sterile implantable device made primarily of human demineralized bone matrix (DBM) (acid extraction of allogeneic bone resulting in loss of most of the mineralized component but retention of proteins) intended to fill bony voids or gaps caused by trauma or surgery, including use in the maxillofacial and/or mandibular bone. The device is bioabsorbable, osteoconductive, and has demonstrated at least potential osteoinductivity for the stimulation of new bone growth. The DBM may be combined with various carrier compounds (e.g., gelatin, hydrogel, starch) or other materials. It is available in the form of powder, crushed granules, putty, chips, or a gel that can be injected through a syringe.


Environmental Conditions

No Data Available


Device Sizes

  • Width: 2.5 Centimeter
  • Length: 5.0 Centimeter
    • Width: 2.5 Centimeter
    • Length: 5.0 Centimeter


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: MQV

    Device Name: Filler, Bone Void, Calcium Compound

    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: 888.3045

    Third Party Flag: N

    Medical Specialty: OR


    Code: MBP

    Device Name: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

    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: 888.3045

    Third Party Flag: N

    Medical Specialty: OR


    Device Identifiers

    Device Id: 00613994985972

    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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