BEUDAMED
    FDA Registration Active 🇺🇸 United States

    RELINE

    Reg #: 3013491327 · FEI: 3013491327 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    NuVasive Manufacturing, LLC
    Registration Number
    3013491327
    FEI Number
    3013491327
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    805 Liberty Lane
    City
    West Carrollton
    State
    OH
    ZIP
    45449
    Country
    US

    Regulatory Submissions

    510(k) Number
    K182974

    Owner / Operator

    Firm Name
    GLOBUS MEDICAL, INC.
    Operator Number
    9056090
    Address
    2560 GENERAL ARMISTEAD AVE., VALLEY FORGE BUSINESS CENTER
    City
    Audubon
    State
    PA
    Postal Code
    19403
    Country
    US
    Correspondent
    DANIEL S PAUL

    Products

    Device Name Product Code
    Appliance, Fixation, Spinal Interlaminal KWP
    Appliance, Fixation, Spinal Intervertebral Body KWQ
    Thoracolumbosacral Pedicle Screw System NKB

    Proprietary Names

    RELINE

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)