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510(k) Data Aggregation

    K Number
    K990381
    Device Name
    TOTALBOND
    Manufacturer
    Date Cleared
    1999-05-17

    (98 days)

    Product Code
    Regulation Number
    872.3275
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    A BURL. CURING ADHESIVE CEMENT INTENDED FOR USE AS A LUTING MATERIAL FOR BONDING INLAYS, ONLAYS, CROWNS, BRIDGES, LAMINATE VENEERS ETC. TO POSTERLY PERFARED TEETH. ALSO INDICATED AS AN AGENT FOR AFFECTING REPAIRS OF TOOTH . COLORED VENEED VENEERS BUNDED TO ATT ECTING READING FOR FREGOUS OR PRECIOUS . FOR THE LATTER, THE KIT CONTAINS A NOBLE METAL PRIMING MATERIAL WHICH SIGNIFICANTLY INCREASES THE BONS STRENGTH OF THE REPAIR. THE KIT ALSO CONTAINS A PORCELAIN PRIMER OF THE IS RECORITIENDED FOR WE IN REBAIRING FRACTURED DENTAL PORCECAINS. IT MEDIATES AN ADHESINE BOND BETWEEN THE PORCECAIN SUBSCRIPTE AND AN OVERLIANG COMPOSITE PESIN.

    Device Description

    Parkell's TOTALBOND is a dual-curing adhesive cement intended for use as a luting material for bonding inlays, onlays, crowns, and bridges to properly prepared teeth. It is also indicated for use as an agent for affecting repairs of tooth-colored veneers bonded to dental alloys, either non-precious or precious. For the latter instance, the supplied kit contains a noble metal-Priming material which significantly increases the bond strength of the repair. The kit also contains a porcelain-primer that is recommended for use in repairing fractured dental porcelains. It mediates an adhesive bond between the porcelain substrate and an overlying composite resin.

    AI/ML Overview

    This document is a 510(k) summary for a dental adhesive resin cement called "TOTALBOND." The information provided does not contain details about acceptance criteria or a study proving that the device meets such criteria. Instead, it is a regulatory document outlining the submission for market clearance, the intended use of the device, and the FDA's decision regarding its substantial equivalence to previously marketed devices.

    Therefore, I cannot provide the requested information as it is not present in the given text.

    The provided text focuses on the administrative and regulatory aspects of the device's submission, such as:

    • Submitter and Contact Information: Parkell Products Inc. and Nelson J. Gendusa, DDS.
    • Submission Date: February 3, 1999.
    • Trade Name and Common Name: TOTALBOND, Adhesive Resin Cement.
    • Classification: Class II, Product Code EMA.
    • Description/Intended Use: Dual-curing adhesive cement for bonding dental restorations (inlays, onlays, crowns, bridges, laminate veneers) and for repairing tooth-colored veneers and fractured dental porcelains.
    • FDA Communication: A letter from the FDA stating that the device is substantially equivalent to predicate devices and can be marketed.
    • Indications for Use: Reiterates the intended uses for bonding and repair.

    To answer your questions, I would need a different type of document, such as a detailed study report, a clinical trial summary, or a sections of the 510(k) submission that specifically address performance testing and acceptance criteria.

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