BEUDAMED
    FDA Registration Active 🇮🇪 Ireland

    Bixcut Reamers

    Reg #: 9616680 · FEI: 3002459190 · Expires 2025
    View on FDA
    Products
    11
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    11

    Registration Details

    Registration Name
    STRYKER IRELAND OSTEONICS
    Registration Number
    9616680
    FEI Number
    3002459190
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Tullagreen Building, IDA Business & Technology Park, Carrigtwohill
    City
    Cork Munster
    Country
    IE

    Regulatory Submissions

    510(k) Number
    K153345

    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
    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer KWZ
    Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous MBL
    Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented KWY
    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented LZO
    Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented LWJ
    Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented JDI
    Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented LPH
    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish MAY
    Prosthesis, Hip, Hemi-, Femoral, Metal KWL
    Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate MEH
    Screw, Fixation, Bone HWC

    Proprietary Names

    Bixcut Reamers Associated instrumentation Stryker Orthopaedics Instruments

    Establishment Types

    Manufacture Medical Device