BEUDAMED
    FDA Registration Active 🇺🇸 United States

    INNESIS PEEK CAGE

    Reg #: 3016244279 · FEI: 3016244279 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BK MEDITECH, USA
    Registration Number
    3016244279
    FEI Number
    3016244279
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    219 Tampico Street
    City
    San Antonio
    State
    TX
    ZIP
    78207
    Country
    US

    Regulatory Submissions

    510(k) Number
    K120464

    Owner / Operator

    Firm Name
    BK Meditech, USA
    Operator Number
    10062179
    Address
    219 Tampico Street
    City
    San Antonio
    State
    TX
    Postal Code
    78207
    Country
    US
    Correspondent
    Katelin McCrady

    Products

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

    Proprietary Names

    INNESIS PEEK CAGE

    Establishment Types

    Repack or Relabel Medical Device