BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NuTech Spine Intervertebral Body Fusion Device

    Reg #: 3009169996 · FEI: 3009169996 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    NUTECH SPINE, INC.
    Registration Number
    3009169996
    FEI Number
    3009169996
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2231 20th Avenue South
    City
    Birmingham
    State
    AL
    ZIP
    35223
    Country
    US

    Regulatory Submissions

    510(k) Number
    K092193

    Owner / Operator

    Firm Name
    NuTech Spine, Inc.
    Operator Number
    10036081
    Address
    600 Luckie Drive, Suite 424
    City
    Birmingham
    State
    AL
    Postal Code
    35223
    Country
    US

    Products

    Device Name Product Code
    Appliance, Fixation, Spinal Intervertebral Body KWQ
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    NuTech Spine Intervertebral Body Fusion Device

    Establishment Types

    Repack or Relabel Medical Device