BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AXS Vecta 74 Intermediate Catheter

    Reg #: 3008853977 · FEI: 3008853977 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    2
    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
    K200206

    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
    Catheter, Percutaneous DQY
    Catheter, Percutaneous, Neurovasculature QJP

    Proprietary Names

    AXS Vecta 74 Intermediate Catheter AXS Vecta 71 Intermediate Catheter

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198