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510(k) Data Aggregation

    K Number
    K182986
    Device Name
    Boston Keratoprosthesis, Type I Lucia
    Manufacturer
    Massachusetts Eye and Ear Infirmary d/b/a Boston
    Date Cleared
    2019-01-30

    (93 days)

    Product Code
    HQM, HOM
    Regulation Number
    886.3400
    Why did this record match?
    Applicant Name (Manufacturer) :

    **Massachusetts Eye **and Ear Infirmary d/b/a Boston

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Boston KPro is indicated to provide a transparent optical pathway through an opacified cornea in an eye that is not a reasonable candidate for any form of corneal transplant, including penetrating keratoplasty.
    Device Description
    The Boston KPro, Type I Lucia is an artificial corneal device that can be used in patients with severe corneal opacity. The device consists of two components: a front plate constructed of clear polymethyl methacrylate (PMMA) plastic, and a back plate constructed of titanium that locks the device in place around a corneal donor graft. The Boston KPro, Type I Lucia is supplied with an assembly tool/pin to assist in device assembly.
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    K Number
    K121203
    Device Name
    BOSTON KERATOPROSTHESIS OR BOSTON KPRO
    Manufacturer
    MASSACHUSETTS EYE & EAR INFIRMARY
    Date Cleared
    2013-05-10

    (385 days)

    Product Code
    HQM
    Regulation Number
    886.3400
    Why did this record match?
    Applicant Name (Manufacturer) :

    **MASSACHUSETTS EYE **& EAR INFIRMARY

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Boston Keratoprosthesis is indicated to provide a transparent optical pathway through an opacified cornea in an eye that is not a reasonable candidate for any form of corneal transplant, including penetrating keratoplasty.
    Device Description
    The Boston Keratoprosthesis is an artificial corneal device that can be used in patients with severe corneal opacity. The Boston Keratoprosthesis is used after standard corneal transplant has failed or when such a transplant would be unlikely to succeed. Thus, keratoprosthesis implantation is a procedure designed to help patients whose conditions are the most difficult to treat. This 510(k) seeks to modify the back plate material from PMMA to titanium. In doing so, the modified implant eliminates the need for a titanium retaining ring which was employed in the predecessors to hold the PMMA back plate in position following implantation. This also simplifies the assembly. It is available in two types. The Type I keratoprosthesis is implanted through and fixed only to the cornea and is used for corneal blindness when the eyelids, blink mechanism and tear film are intact. The Type II keratoprosthesis has an anterior extension to enable implantation through an opening in the closed eyelids. The Type II device is used in eyes with severe dry eye, mucosal keratinization and obliteration of the normal conjunctival fornices, such as after severe chemical injuries or Stevens Johnson syndrome or mucous membrane pemphigoid. Both devices are identical in terms of assembly.
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