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510(k) Data Aggregation

    K Number
    K002586
    Device Name
    MEDPOR PTERIONAL SURGICAL IMPLANT
    Manufacturer
    POREX SURGICAL PRODUCTS GROUP
    Date Cleared
    2000-11-17

    (88 days)

    Product Code
    MNF
    Regulation Number
    878.3550
    Why did this record match?
    Applicant Name (Manufacturer) :

    POREX SURGICAL PRODUCTS GROUP

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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