BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Target 360 Ultra

    Reg #: 3008853977 · FEI: 3008853977 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    10
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Stryker Neurovascular
    Registration Number
    3008853977
    FEI Number
    3008853977
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    47900 Bayside Parkway
    City
    Fremont
    State
    CA
    ZIP
    94538
    Country
    US

    Regulatory Submissions

    510(k) Number
    K153658

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Device, Vascular, For Promoting Embolization KRD
    Device, Neurovascular Embolization HCG

    Proprietary Names

    Target 360 Ultra Target 360 Standard Target Helical Nano Target XL 360 Standard Target 360 Nano Target Helical Ultra Target XL Helical Target XL 360 Soft Target 3D Target 360 Soft

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility