BEUDAMED
    FDA Registration Active 🇮🇪 Ireland

    Active-X Inlay Patella Component

    Reg #: 3014763043 · FEI: 3014763043 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Signature Orthopaedics Europe Ltd
    Registration Number
    3014763043
    FEI Number
    3014763043
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Unit A, IDA Business & Technology Park, Garrycastle
    City
    Athlone Westmeath
    Country
    IE

    Regulatory Submissions

    510(k) Number
    K160159

    Owner / Operator

    Firm Name
    Signature Orthopaedics Pty Limited
    Operator Number
    10037793
    Address
    7 Sirius Road
    City
    Lane Cove West
    State
    New South Wales
    Postal Code
    2066
    Country
    AU
    Correspondent
    Declan P Brazil

    Products

    Device Name Product Code
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer JWH
    Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer MBH

    Proprietary Names

    Active-X Inlay Patella Component Active-X Cemented Femoral Component Active-X Ultracongruent Meniscal Insert Active-X Regular Meniscal Insert Active-X Patella Component Active-X Cemented Tibial Component Active-X Ultracongruent+ Meniscal Insert

    Establishment Types

    Manufacture Medical Device