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510(k) Data Aggregation

    K Number
    K972319
    Device Name
    AURECAST GF
    Date Cleared
    1997-08-26

    (67 days)

    Product Code
    Regulation Number
    872.3060
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Dental casting alloy for making restoration. (NOT FOR USE WITH DENTAL PORCELAIN )

    Device Description

    Silver-palladium based casting alloy

    AI/ML Overview

    The document provided is a 510(k) premarket notification for a dental casting alloy, not a medical device that utilizes an algorithm or AI. Therefore, the concepts of acceptance criteria for algorithm performance, study design with human readers, ground truth, and training/test sets are not applicable.

    The "acceptance criteria" in this context refer to the demonstration of substantial equivalence to a legally marketed predicate device, based on similar technological characteristics (composition, physical, and mechanical properties) and intended use.

    Here's the information extracted from the document, rephrased to fit the context of device equivalence rather than algorithm performance:

    1. A table of acceptance criteria and the reported device performance

    The acceptance criteria are implicitly defined by the properties of the legally marketed predicate device, Jelenko Albacast. The new device, Aurecast GF, is deemed to meet these criteria if its properties are substantially similar, especially for critical attributes.

    PropertyPredicate Device (Albacast)New Device (Aurecast GF)Acceptance Criterion (Implicitly "Substantially Similar")
    Composition (weight%)
    Ag7072.1Concentration difference
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