BEUDAMED
    FDA Registration Active 🇫🇷 France

    JULIET

    Reg #: 3010658151 · FEI: 3010658151 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Alpes CN
    Registration Number
    3010658151
    FEI Number
    3010658151
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Immeuble ABC3, 80 rue Douglas Engelbart,, Archamps Technopole,
    City
    Archamps Haute-Savoie
    Country
    FR

    Regulatory Submissions

    510(k) Number
    K081888

    Owner / Operator

    Firm Name
    SPINEART SA
    Operator Number
    10028947
    Address
    Chemin du Pre-Fleuri 3
    City
    Plan-les-Ouates
    State
    Geneve
    Postal Code
    1228
    Country
    CH
    Correspondent
    Max LOK

    Products

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

    Proprietary Names

    JULIET

    Establishment Types

    Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device