BEUDAMED
    FDA Registration Active 🇫🇷 France

    PL2-CM088

    Reg #: 3003526896 · FEI: 3003526896 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    61
    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
    K223251

    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 Bone Graft, Lumbar MAX

    Proprietary Names

    PL2-CM088 PL2-CM100 PL2-CM135 PL2-CM165 PL2-CS115 PL2-CM150 PL2-CS100 PL2-CM108 PL2-CM160 PL2-CM145 PL2-CM158 PL2-CM130 PL2-CM090 PL2-CS120 PL2-CS108 PL2-CS078 PL2-CM070 PL2-CM140 PL2-CM155 PL2-CM120 PL2-CM110 PL2-CS110 PL2-CS160 PL2-CS085 PL2-CS130 PL2-CS125 PL2-CS080 PL2-CS128 PL2-CM075 PL2-CS070 PL2-CS140 PL2-CM098 PL2-CS098 PL2-CS090 PL2-CM080 PL2-CS145 PL2-CM105 PL2-CM095 PL2-CS135 PL2-CM168 Hexanium® PLIF PL2-CM078 PL2-CS158 PL2-CM118 PL2-CS138 PL2-CM128 PL2-CM138 PL2-CM115 PL2-CM125 PL2-CS155 PL2-CS095 PL2-CS088 PL2-CS168 PL2-CS148 PL2-CS075 PL2-CS105 PL2-CS118 PL2-CS165 PL2-CM085 PL2-CM148 PL2-CS150

    Establishment Types

    Manufacture Medical Device