BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Curiteva Porous PEEK Lumbar Interbody Fusion System

    Reg #: 3012131184 · FEI: 3012131184 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CURITEVA, INC.
    Registration Number
    3012131184
    FEI Number
    3012131184
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    25127 WILL MCCOMB DR
    City
    Tanner
    State
    AL
    ZIP
    35671
    Country
    US

    Regulatory Submissions

    510(k) Number
    K233744

    Owner / Operator

    Firm Name
    Curiteva, Inc.
    Operator Number
    10050404
    Address
    25127 Will McComb Drive
    City
    Tanner
    State
    AL
    Postal Code
    35671
    Country
    US
    Correspondent
    Scott L Steelman

    Products

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

    Proprietary Names

    Curiteva Porous PEEK Lumbar Interbody Fusion System

    Establishment Types

    Manufacture Medical Device