BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Journey II UK Knee System

    Reg #: 1020279 · FEI: 1020279 · Expires 2025
    View on FDA
    Products
    7
    Proprietary Names
    10
    Establishment Types
    1
    Classifications
    7

    Registration Details

    Registration Name
    SMITH & NEPHEW, INC.
    Registration Number
    1020279
    FEI Number
    1020279
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1450 BROOKS RD.
    City
    MEMPHIS
    State
    TN
    ZIP
    38116
    Country
    US

    Regulatory Submissions

    510(k) Number
    K230653

    Owner / Operator

    Firm Name
    Smith & Nephew, Inc.
    Operator Number
    1020279
    Address
    2875 Railroad Street
    City
    Pittsburgh
    State
    PA
    Postal Code
    15222
    Country
    US
    Correspondent
    Lisa Ewing

    Products

    Device Name Product Code
    Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer KRR
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive OIY
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer JWH
    Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer MBH
    Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer KRO
    Prosthesis, Toe, Constrained, Polymer KWH
    Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer HSX

    Proprietary Names

    Journey II UK Knee System JOURNEY II Uni Knee System Genesis Uni Knee System JOURNEY PFJ System JOURNEY II XR Bi-Cruciate Retaining Knee System JOURNEY Uni Knee System Legion Hinge Total JOURNEY BCS and II Knee Systems JOURNEY II CR Knee System ANTHEM Total Knee System

    Establishment Types

    Manufacture Medical Device