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    FDA Registration Active 🇺🇸 United States

    Pak 9733497 NAV NIM-SPINE PEDICLE ACC KIT

    Reg #: 1225492 · FEI: 3001237338 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    NextPhase Medical Devices LLC
    Registration Number
    1225492
    FEI Number
    3001237338
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    88 Airport Dr
    City
    ROCHESTER
    State
    NH
    ZIP
    03867
    Country
    US

    Regulatory Submissions

    510(k) Number
    K131425

    Owner / Operator

    Firm Name
    NextPhase Medical Devices LLC
    Operator Number
    9026654
    Address
    88 AIRPORT DR.
    City
    Rochester
    State
    NH
    Postal Code
    03867
    Country
    US
    Correspondent
    James G Bennett

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX
    Orthopedic Stereotaxic Instrument OLO

    Proprietary Names

    Pak 9733497 NAV NIM-SPINE PEDICLE ACC KIT PAK 9733498NAV NAVIGATED PEDICLE ACCESS Kit PAK 9733498 NAVIGATED PEDICLE ACCESS KIT PAK 9733497NAV NAV NIM-SPINE PEDICLE ACCESS KIT

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)