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510(k) Data Aggregation

    K Number
    K152476
    Date Cleared
    2016-02-09

    (162 days)

    Product Code
    Regulation Number
    878.4010
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Exofin High Viscosity Tissue Adhesive

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Exofin® High Viscosty Tissue Adhesive is intended for topical application only to hold closed easily approximated skin edges of wounds from surgical incisions from minimally invasive surgery, and simple, thoroughly cleansed, trauma-induced lacerations.

    Exofin® High Viscosity Tissue Adhesive may be used in conjunction with, but not in place of, deep dermal sutures.

    Device Description

    Exofin® High Viscosity Tissue Adhesive is a sterile, liquid topical skin adhesive containing a monomeric (2-octyl cyanoacrylate) formulation and the colorant D & C Violet #2. It is provided in a single use aluminum collapsible tube packaged in a RXM 48gaPET-200LDPE Film/1059B uncoated Tyvek pouch containing an applicator. The applicator is comprised of a self-puncturing cap and a soft elastomeric brush, which allows the adhesive to spread uniformly. As applied to skin, the liquid is syrup-like in viscosity and polymerizes within minutes. Exofin® High Viscosity Tissue Adhesive has a syrup-like viscosity. The increased viscosity is intended to reduce the risk of unintended placement of the adhesive during application due to migration of the liquid adhesive from the wound site. In vitro studies have shown that Exofin®High Viscosity Tissue Adhesive acts as a barrier to microbial penetration as long as the adhesive film remains intact. Clinical studies were not conducted to demonstrate microbial barrier properties and a correlation between microbial barrier properties and a reduction in infection have not been established.

    AI/ML Overview

    This document is a 510(k) premarket notification for the Exofin® High Viscosity Tissue Adhesive. It does not describe acceptance criteria or a study proving that an AI-powered device meets acceptance criteria. Instead, it describes performance testing for a medical device (a tissue adhesive) against established ASTM standards and biocompatibility in accordance with ISO 10993-1.

    Therefore, I cannot provide the requested information regarding acceptance criteria and an AI study.

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