BEUDAMED
    FDA Registration Active 🇺🇸 United States

    InterFuse DA Intervertebral Body Fusion Device

    Reg #: 3010020754 · FEI: 3010020754 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    NEXT ORTHOSURGICAL
    Registration Number
    3010020754
    FEI Number
    3010020754
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3270 Corporate Vw Ste A
    City
    Vista
    State
    CA
    ZIP
    92081
    Country
    US

    Regulatory Submissions

    510(k) Number
    K110045

    Owner / Operator

    Firm Name
    Next Orthosurgical
    Operator Number
    10042957
    Address
    3270 Corporate View, Suite A
    City
    Vista
    State
    CA
    Postal Code
    92081
    Country
    US
    Correspondent
    Misty Calkins

    Products

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

    Proprietary Names

    InterFuse DA Intervertebral Body Fusion Device

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device