BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AXS Vecta 46 Intermediate Catheter

    Reg #: 3012497308 · FEI: 3012497308 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Stryker US Supply Chain Operations
    Registration Number
    3012497308
    FEI Number
    3012497308
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1551 Perry Rd Ste 101
    City
    Plainfield
    State
    IN
    ZIP
    46168
    Country
    US

    Regulatory Submissions

    510(k) Number
    K202752

    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, Neurovasculature QJP

    Proprietary Names

    AXS Vecta 46 Intermediate Catheter

    Establishment Types

    Repack or Relabel Medical Device