Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K220791
    Manufacturer
    Date Cleared
    2022-05-03

    (46 days)

    Product Code
    Regulation Number
    880.6850
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Surgical and Prosthetic Trays are intended for organizing, sterilizing and storing of instruments. The Surgical and Prosthetic Trays are not intended to maintain sterility and are to be used in conjunction with a legally marketed, validated sterilization pouch.

    Device Description

    The proposed Surgical and Prosthetic Trays are reusable perforated containers that are intended to store and organize the instruments needed before, during and after implant surgery and the prosthetic procedure as well as hold instruments during sterilization.

    The Trays are containers composed of three main components: a lid, a base and an overlay, which are all made of polyphenylsulfone (Radel R5000NT). The trays have co-molded silicone tooling supports and silicone rubber grommets to hold instruments. The base and overlay are custom printed to indicate the guided surgery or prosthetic procedure workflow and the position of the instruments within the tray for the different product lines.

    The proposed Surgical and Prosthetic Trays are available in two tray sizes. The Surgical trays are available in medium size with outer dimensions of 7.3 x 5.5 x 2.4 inches and the Prosthetic trays are available in small size with outer dimensions of 5.4 x 3.9 x 2.4. Each tray size is offered in 2 inner tray configurations with varied instrument loads, see Table 1.

    AI/ML Overview

    The provided text describes the acceptance criteria and the studies that prove the device meets these criteria for "Surgical and Prosthetic Trays" (K220791).

    Here's a breakdown of the requested information:

    1. Table of Acceptance Criteria and Reported Device Performance

    Test NameTest MethodologyAcceptance CriteriaReported Device Performance
    Sterilization cycle validationANSI/AAMI/ISO 17665-1:2006/(R)2013, ISO 17665-2:2009Sterility assurance level (SAL) of ≤ 10-6Pass
    Drying validationAAMI TIR12:2020, ANSI/AAMI/ISO 17665-2:2009No visible moisture, ≤ 3% weight gain of packaging and absorbable materialsPass
    Cleaning (Manual Pre-Cleaning and automated Cleaning)AAMI TIR 30:2011, ISO 15883-1:2014No visible soil.
    Protein and TOC content Limit
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1