Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K183506
    Date Cleared
    2019-02-14

    (58 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The HEALIX ADVANCE Anchor is indicated for use in soft tissue to bone fixation with post-operative immobilization as follows:
    Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction
    Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair
    Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis
    Elbow: Biceps Tendon Reattachment, Ulnar Collateral Ligament Reconstruction, Radial Collateral Ligament Reconstruction
    Hip: Capsular Repair, Acetabular Labral Repair

    Device Description

    The HEALIX ADVANCETM Anchor with DYNACORDTM Suture is a threaded suture anchor preloaded on a disposable inserter assembly. HEALIX ADVANCETM Anchors with DYNACORDTM Suture are available in absorbable BR and non-absorbable PEEK materials. Devices with needles will be offered to facilitate suture passage through tissue. The HEALIX ADVANCETM Anchor with DYNACORDTM Suture is provided sterile and is for single use only.

    AI/ML Overview

    The provided text is a 510(k) summary for the HEALIX ADVANCE™ Anchor with DYNACORD™ Suture. It describes the device, its intended use, and substantial equivalence to predicate devices, supported by non-clinical testing. However, it does not contain information related to a study proving a device meets acceptance criteria for an AI/algorithm-based medical device performance.

    Specifically, the document discusses a suture anchor (a physical medical device used in orthopedic surgery), not an image-based AI or algorithm. Therefore, the requested information (acceptance criteria for an AI, sample sizes for AI test/training sets, expert ground truth establishment, MRMC studies, standalone AI performance) is not applicable to this document.

    The "studies" mentioned in the document are non-clinical physical tests of the suture anchor and suture, such as:

    • suture diameter
    • knot tensile strength
    • suture approximation force
    • chemical characterization
    • anchor fixation (in-vitro and in-vivo)
    • torque testing
    • biocompatibility
    • sterility
    • packaging
    • shelf-life
    • bacterial endotoxin testing

    These tests are to demonstrate the physical properties and safety of the orthopedic implant and suture, not the performance of an AI algorithm.

    Therefore, I cannot provide the requested table or details about an AI study based on the provided text.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1