BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    Lateralized and Augmented Baseplates

    K Number: K210790 · Decision Aug 25, 2021
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    203
    Applicant Total
    11
    Review Days
    162

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    Basic Information

    Device Name
    Lateralized and Augmented Baseplates
    K Number
    K210790
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3660
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Fx Shoulder USA, Inc.
    Date Received
    March 16, 2021
    Decision Date
    August 25, 2021
    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 Fx Shoulder USA, Inc.

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