BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Keos Lumbar IBFD

    Reg #: 3013921069 · FEI: 3013921069 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    KEOS
    Registration Number
    3013921069
    FEI Number
    3013921069
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1824 COLONIAL VILLAGE LN
    City
    Lancaster
    State
    PA
    ZIP
    17601
    Country
    US

    Regulatory Submissions

    510(k) Number
    K163386

    Owner / Operator

    Firm Name
    Keos
    Operator Number
    10055802
    Address
    1824 Colonial Village Lane
    City
    Lancaster
    State
    PA
    Postal Code
    17601
    Country
    US
    Correspondent
    Scott Peterson

    Products

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

    Proprietary Names

    Keos Lumbar IBFD

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility