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510(k) Data Aggregation

    K Number
    K003951
    Device Name
    PECTOFIX STERNAL REPAIR WIRE
    Manufacturer
    PECTOFIX, INC.
    Date Cleared
    2001-03-21

    (90 days)

    Product Code
    JDQ
    Regulation Number
    888.3010
    Why did this record match?
    Applicant Name (Manufacturer) :

    PECTOFIX, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000694
    Device Name
    PECTOFIX DYNAMIC STERNAL FIXATION SYSTEM (DSF)
    Manufacturer
    PECTOFIX, INC.
    Date Cleared
    2000-05-11

    (71 days)

    Product Code
    JDQ
    Regulation Number
    888.3010
    Why did this record match?
    Applicant Name (Manufacturer) :

    PECTOFIX, INC.

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

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