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510(k) Data Aggregation

    K Number
    K982439
    Device Name
    PROXIDERM, MODELS TN 460, TN 90 460, BK 460
    Manufacturer
    PROGRESSIVE SURGICAL PRODUCTS, INC.
    Date Cleared
    1998-09-08

    (56 days)

    Product Code
    MKY
    Regulation Number
    878.4320
    Why did this record match?
    Applicant Name (Manufacturer) :

    PROGRESSIVE SURGICAL PRODUCTS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Proxiderm is intended to be utilized prior to a surgical procedure to remove a defect or prior to implantation of a prosthesis to provide additional skin for coverage of the defect or prosthesis.
    Device Description
    Not Found
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    K Number
    K970439
    Device Name
    PROXIDERM (D-460,D 90 460,D 180,460, PS 460)
    Manufacturer
    PROGRESSIVE SURGICAL PRODUCTS, INC.
    Date Cleared
    1997-04-16

    (70 days)

    Product Code
    MKY
    Regulation Number
    878.4320
    Why did this record match?
    Applicant Name (Manufacturer) :

    PROGRESSIVE SURGICAL PRODUCTS, INC.

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

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