BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    VANGUARD 360 REVISION KNEE SYSTEM

    Reg #: 3012392319 · FEI: 3012392319 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Zimmer Biomet Canada DFE
    Registration Number
    3012392319
    FEI Number
    3012392319
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2323 Argentia Road
    City
    Mississauga Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K093293

    Owner / Operator

    Firm Name
    ZIMMER, INC.
    Operator Number
    1822565
    Address
    345 E. Main Street, --
    City
    Warsaw
    State
    IN
    Postal Code
    46580
    Country
    US

    US Agent

    Business Name
    Zimmer Biomet
    Contact Name
    Holly Seppanen
    Address
    1800 West Center Street
    City
    Warsaw
    State
    IN
    ZIP
    46580
    Country
    US
    Email
    [email protected]
    Phone
    952 8470494

    Products

    Device Name Product Code
    Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer MBV
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer JWH

    Proprietary Names

    VANGUARD 360 REVISION KNEE SYSTEM

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device