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510(k) Data Aggregation

    K Number
    K081396
    Manufacturer
    Date Cleared
    2009-01-14

    (240 days)

    Product Code
    Regulation Number
    872.3630
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SWISSPLANT DENTAL IMPLANT SYSTEM

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

    The SwissPlant Dental Implant system consists of two-piece implants for one or two-stage surgical procedures that are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations including: cement retained, screw retained or overdenture restorations and in terminal or immediate abutment support for fixed bridgework. The SwissPlant dental implants are intended for immediate placement and function on single tooth and/or multiple tooth applications recognizing initial implant stability and appropriate occlusal loading, to restore normal masticatory function.

    Device Description

    The SwissPlant Dental implant system consists of implants, abutments, healing components, fixation screws and surgical armamentaria for use in one or twostage placement and restorations.

    AI/ML Overview

    I am sorry, but the provided text does not contain any information about acceptance criteria or a study proving that a device meets those criteria. The document is a 510(k) summary and an FDA clearance letter for a dental implant system. It describes the device, its intended use, and its substantial equivalence to a predicate device, but it does not detail any performance studies against specific acceptance criteria.

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