BEUDAMED
    FDA Registration Active 🇨🇭 Switzerland

    3.2mmX26mm TWINFIX COMP. SCREW

    Reg #: 8031020 · FEI: 3002807830 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    15
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STRYKER GmbH
    Registration Number
    8031020
    FEI Number
    3002807830
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    BOHNACKERWEG 1
    City
    SELZACH Solothurn
    Country
    CH

    Regulatory Submissions

    510(k) Number
    K013775

    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
    Plate, Fixation, Bone HRS

    Proprietary Names

    3.2mmX26mm TWINFIX COMP. SCREW 3.2mmX32mm TWINFIX COMP. SCREW 3.2mmX18mm TWINFIX COMP. SCREW 3.2mmX27mm TWINFIX COMP. SCREW 3.2mmX20mm TWINFIX COMP. SCREW 3.2mmX16mm TWINFIX COMP. SCREW 3.2mmX30mm TWINFIX COMP. SCREW 3.2mmX34mm TWINFIX COMP. SCREW 3.2mmX24mm TWINFIX COMP. SCREW 3.2mmX14mm TWINFIX COMP. SCREW 3.2mmX23mm TWINFIX COMP. SCREW 3.2mmX28mm TWINFIX COMP. SCREW 3.2mmX22mm TWINFIX COMP. SCREW 3.2mmX25mm TWINFIX COMP. SCREW 3.2mmX21mm TWINFIX COMP. SCREW

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility