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510(k) Data Aggregation

    K Number
    K024041
    Device Name
    ZETAPLUS SOFT
    Manufacturer
    Date Cleared
    2002-12-18

    (12 days)

    Product Code
    Regulation Number
    872.3660
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Zhermack ZETAPLUS SOFT a dental impression material intended to be placed on a preformed impression tray and used to reproduce the structure of a patient's teeth and gums. ZETAPLUS SOFT is material for preliminary impression (first impression).

    Device Description

    Not Found

    AI/ML Overview

    This FDA 510(k) clearance letter for the Zetaplus Soft dental impression material does not contain the detailed information requested regarding acceptance criteria and study data.

    The document is a clearance letter, confirming that the device is substantially equivalent to legally marketed predicate devices. It provides:

    • Trade/Device Name: Zetaplus Soft
    • Regulation Number and Name: 872.3660, Impression Material
    • Regulation Class: II
    • Product Code: ELW
    • Indications for Use: "Zhermack ZETAPLUS SOFT a dental impression material intended to be placed on a preformed impression tray and used to reproduce the structure of a patient's teeth and gums. ZETAPLUS SOFT is material for preliminary impression (first impression)."

    However, it does not include any studies, performance data, or acceptance criteria in the format requested. These details would typically be found in the 510(k) submission itself, which is a much larger technical document not included in this clearance letter.

    Therefore, I cannot populate the table or answer the specific questions about the study from the provided text.

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