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510(k) Data Aggregation

    K Number
    K231210
    Device Name
    DGA Abutment
    Date Cleared
    2024-03-05

    (313 days)

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

    K151295, K142813

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

    DGA Abutment is a patient-specific prosthetic component directly connected to the endosseous dental implant (details as below) and is intended for use as a support for single or multiple tooth prostheses in the maxilla or mandible of a partially or fully edentulous patient.

    Device Description

    DGA Abutment is endosseous implant abutment which is placed into a corresponding dental implant to provide support for a prosthetic restoration. DGA Abutment is made of titanium grade Ti-6Al-4V ELI (meets ASTM Standard F136). The DGA Abutment is mounted on the implant with a screw. Each abutment is supplied with two identical screws which are used for:
    a. For fixing into the endosseous implant.
    b. For dental laboratory use during fabrication of restoration.
    The screw is also made of titanium grade Ti-6AI-4V ELI (meets ASTM Standard F136).

    AI/ML Overview

    The provided text is a 510(k) summary for the DGA Abutment, a dental implant component. It addresses substantial equivalence rather than presenting an AI/ML device study with acceptance criteria and performance data. Therefore, the document does not contain the information requested regarding acceptance criteria, study details, sample sizes, expert involvement, or MRMC studies for an AI/ML device.

    The document discusses the mechanical properties and biocompatibility of the DGA Abutment, comparing it to predicate devices. It states that fatigue testing was conducted according to ISO 14801:2016 and FDA guidance, and biocompatibility testing was done as per ISO 10993 series. However, it does not provide specific acceptance criteria or reported performance data in a table format for these tests, nor does it refer to an AI/ML algorithm.

    Therefore, I cannot directly answer your prompt using the provided text. The prompt's questions pertain to acceptance criteria and study methodologies for an AI/ML device, which are not found in this 510(k) submission for a physical dental abutment.

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