Search Results
Found 2 results
510(k) Data Aggregation
K Number
K182986Device 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
886.3400Why 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.
Ask a Question
K Number
K121203Device Name
BOSTON KERATOPROSTHESIS OR BOSTON KPRO
Manufacturer
MASSACHUSETTS EYE & EAR INFIRMARY
Date Cleared
2013-05-10
(385 days)
Product Code
HQM
Regulation Number
886.3400Why 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.
Ask a Question
Page 1 of 1