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510(k) Data Aggregation
K Number
K223074Device Name
CorNeat EverPatch
Manufacturer
Date Cleared
2023-06-02
(245 days)
Product Code
Regulation Number
886.3130Why did this record match?
Product Code :
QWU
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The CorNeat EverPatch is intended for implantation to reinforce sclera and aid the physical reconstruction of the ocular surface.
Device Description
The CorNeat EverPatch is a synthetic, tissue-integrating surgical matrix made of non-degradable polymer fibers. The EverPatch includes 6 bio-stitching holes which are intended to anchor the device by facilitating direct conjunctival adhesion to the sclera thus supporting its bio-integration. The holes at each corner can also be used to suture the device to the sclera.
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