BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

    Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid

    K Number: K241491 · Decision Oct 10, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    203
    Applicant Total
    2
    Review Days
    139

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    Basic Information

    Device Name
    Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid
    K Number
    K241491
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3660
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Stryker Corporation (Tornier, S.A.S.)
    Date Received
    May 24, 2024
    Decision Date
    October 10, 2024
    Product Code
    PHX
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    PHX Shoulder Prosthesis, Reverse Configuration

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    Other Clearances by Stryker Corporation (Tornier, S.A.S.)

    K Number Device Name
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