BEUDAMED
    FDA Registration Active 🇺🇸 United States

    PLIF Peek Implant

    Reg #: 3010143171 · FEI: 3010143171 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    AR FABRICATING
    Registration Number
    3010143171
    FEI Number
    3010143171
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    40132 Industrial Park Cir Ste 102
    City
    Georgetown
    State
    TX
    ZIP
    78626
    Country
    US

    Regulatory Submissions

    510(k) Number
    K170572

    Owner / Operator

    Firm Name
    AR Fabricating
    Operator Number
    10043437
    Address
    40132 Industrial park Cir., suite 102
    City
    Georgetown
    State
    TX
    Postal Code
    78626
    Country
    US
    Correspondent
    Thomas Siemer

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    PLIF Peek Implant Lateral Peek Implant Cervical Peek Implant TLIF Peek Implant

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)