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510(k) Data Aggregation

    K Number
    K180859
    Date Cleared
    2018-12-13

    (255 days)

    Product Code
    Regulation Number
    872.3640
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    PYRAMIDION Dental Implants and Prostheses

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

    DenTack PYRAMIDION Dental Implants and Prostheses are intended for surgical placement in the maxilla and/or in the mandible to provide a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous jaws utilizing conventional, delayed or immediate loading when good primary stability is achieved and with appropriate occlusal loading. Implants in 5-6mm length are indicated for delayed loading only.

    Device Description

    DenTack has developed a range of expandable dental implants made of titanium (the most common material for dental implants) to serve the need of patients that require partial or complete tooth restoration.

    The implant is placed so its end is in the trabecular (spongy) bone like any other implant. Once in place, the apical portion of the implant is expanded to achieve increased contact surface area with the surrounding bone.

    The system also includes various accessories that are attached to the implant. The PYRAMIDION has an external hex connection with 0.7mm height and 2.7mm hex with a distinct projection externally to the implant body. The connection between the prosthetic part to the upper platform of the implant interacts with a recessed plain of 15-degrees into the upper platform of the implant body while it is projected from the prosthetic part.

    All DenTack's implants are made of biocompatible Titanium. Prostheses and Surgical components are made of same Titanium alloy, stainless-steel and polymers.

    DenTack's PYRAMIDION Implants with are the subject of this submission are available in outer diameter (OD) of 4.1 mm and in length of 5 and 6 mm.

    DenTack's Prostheses and dimension ranges are identified as follows:
    Metal Housing: 3.3 mm Height
    Plastic Cup: 2.7 mm Height
    Straight Multi-Unit Sleeve: 11 mm Height
    Straight Multi-Unit Screw: 2.3 mm Diameter
    Angled Abutments 15° And 22.5°: Length: 7 mm – 9 mm
    Angled Abutments 15° Large: Total Length: 9 mm – 12 mm
    Ball Attachments: 2, 3 and 4 mm Height
    Direct Screw Platform
    Straight Abutments 2, 3, 8.5 mm Length
    Straight Multi-Unit Abutments 2, 3 and 4 mm Length
    Angled Multi Unit Abutments 17° and 1.5 and 3 mm Length
    Healing Caps 3, 4, 5 and 6 mm
    Cover Screw

    The Direct Screw Platform is to be used with a burn-out plastic sleeve for ensuring a minimum post height of 4 mm (with no angular correction).

    Like the QUAD implants cleared under K152188, the subject PYRAMIDION implants expansion is performed using a reusable Expansion Tool and Ratchet Torque).

    AI/ML Overview

    The provided text is a 510(k) summary for the DenTack PYRAMIDION Dental Implants and Prostheses. It describes the device, its intended use, and comparative testing performed to demonstrate substantial equivalence to predicate devices. However, this document does not describe a study involving an AI/Machine Learning device or its acceptance criteria and performance metrics.

    The document primarily focuses on mechanical, physical, and biocompatibility testing of dental implants and prostheses, comparing them to legally marketed predicate devices. It covers aspects like:

    • Fatigue testing (ISO 14801): To assess durability.
    • Surface analysis (SEM): To characterize the implant surface.
    • Implant removal after expansion: To evaluate interaction with artificial bone.
    • Minimal rotation torque after placement and expansion: To assess stability.
    • Partially expanded implant reciprocating effect test: To evaluate effects of rotation.
    • Biocompatibility (ISO 10993): To ensure biological safety.
    • Sterilization validation (Gamma and Steam): To ensure sterility.
    • Cleaning validation: For reusable tools.
    • Shelf life validation: To confirm sterility maintenance over time.
    • Comparative pull-out test (ASTM F543): To assess mechanical strength.
    • Comparative bone to implant contact surface area analysis: To compare integration potential.
    • Implant surface area analysis: For physical characteristics comparison.

    Therefore, I cannot provide the requested information regarding AI/ML device acceptance criteria and performance, as the document does not contain any details about an AI/ML component or study.

    The questions posed (e.g., sample size for test set, number of experts for ground truth, MRMC study, standalone algorithm performance) are highly specific to AI/Machine Learning model validation in a medical context, which is not described in this 510(k) summary for dental implants.

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