BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

    Reg #: 3011577940 · FEI: 3011577940 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Titan Spine, a Division of Medtronic
    Registration Number
    3011577940
    FEI Number
    3011577940
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    8347 N Steven Rd
    City
    Milwaukee
    State
    WI
    ZIP
    53223
    Country
    US

    Regulatory Submissions

    510(k) Number
    K201267

    Owner / Operator

    Firm Name
    Medtronic, Inc.
    Operator Number
    2112641
    Address
    710 Medtronic Parkway
    City
    Minneapolis
    State
    MN
    Postal Code
    55432
    Country
    US

    Products

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

    Proprietary Names

    Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

    Establishment Types

    Manufacture Medical Device