BEUDAMED
    FDA Registration Active 🇫🇷 France

    AC2-SD3816S

    Reg #: 3003526896 · FEI: 3003526896 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    57
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SPINEVISION SAS
    Registration Number
    3003526896
    FEI Number
    3003526896
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3 Rue De La Renaissance
    City
    Antony Hauts-de-Seine
    Country
    FR

    Regulatory Submissions

    510(k) Number
    K221578

    Owner / Operator

    Firm Name
    SPINEVISION SAS
    Operator Number
    9048013
    Address
    3 rue de la Renaissance
    City
    Antony
    State
    Paris
    Postal Code
    F-92160
    Country
    FR
    Correspondent
    Quang TRAN

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Integrated Fixation, Cervical OVE

    Proprietary Names

    AC2-SD3816S AC2-CSM05C AC2-CSM09L AC2-CSS05L AC2-CSL08C AC2-CSS06C AC2-CSM12C AC2-CSS07C AC2-CSS11L AC2-CSL12L AC2-CSM11L AC2-CSL12C AC2-CSL05C AC2-CSM10C AC2-CSS12C AC2-CSS10C AC2-CSM06L AC2-SD3812S AC2-CSS09L AC2-CSS08C AC2-CSM09C AC2-CSM08L AC2-CSM07C AC2-SD3810S AC2-CSM07L AC2-CSM06C AC2-CSM10L AC2-CSS10L AC2-CSS07L AC2-SD3510S AC2-SD3514S AC2-CSM08C AC2-CSS11C AC2-SD3516S AC2-CSL08L AC2-SD3814S AC2-CSS12L AC2-CSL11C Hexanium® ACIF AC2-CSM12L AC2-CSL07C AC2-CSL05L AC2-CSM05L AC2-CSS08L AC2-CSL07L AC2-CSL10C AC2-CSL06L AC2-CSS06L AC2-CSL09L AC2-CSL09C AC2-CSL10L AC2-SD3512S AC2-CSS09C AC2-CSS05C AC2-CSL11L AC2-CSL06C AC2-CSM11C

    Establishment Types

    Manufacture Medical Device