BEUDAMED
    FDA Registration Active 🇨🇭 Switzerland

    CURE ACP 2

    Reg #: 3007728266 · FEI: 3007728266 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    SPINEART SA
    Registration Number
    3007728266
    FEI Number
    3007728266
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Chemin du Pre-Fleuri 3
    City
    Plan-les-Ouates Geneve
    Country
    CH

    Regulatory Submissions

    510(k) Number
    K210286

    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
    Appliance, Fixation, Spinal Intervertebral Body KWQ

    Proprietary Names

    CURE ACP 2

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility