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510(k) Data Aggregation

    K Number
    K955511
    Device Name
    ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP
    Manufacturer
    JOINT MEDICAL PRODUCTS CORP.
    Date Cleared
    1996-02-26

    (84 days)

    Product Code
    LPH
    Regulation Number
    888.3358
    Why did this record match?
    Applicant Name (Manufacturer) :

    JOINT MEDICAL PRODUCTS CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K954935
    Device Name
    S-ROM FEMORAL HIP STEM - SIZE 14 X 8
    Manufacturer
    JOINT MEDICAL PRODUCTS CORP.
    Date Cleared
    1996-01-22

    (87 days)

    Product Code
    LPH
    Regulation Number
    888.3358
    Why did this record match?
    Applicant Name (Manufacturer) :

    JOINT MEDICAL PRODUCTS CORP.

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

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