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510(k) Data Aggregation

    K Number
    K080447
    Manufacturer
    Date Cleared
    2008-06-13

    (115 days)

    Product Code
    Regulation Number
    888.3040
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SURGICRAFT SCREW FIXATION SYSTEM

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

    The Surgicraft Screw Fixation System and is a single-use, soft tissue anchor which will be used to secure soft tissue to bone during reconstructive surgery. The anchor is intended for use in such procedures as: Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Acromio-Clavicular Separation Repair, Capsular Shift/Capsulolabral Reconstruction, Biceps Tenodesis, Deltoid Repair. Foot and Ankle: Medial Instability Repair/Reconstruction, Lateral Instability Repair/Reconstruction, Achilles Tendon Repair/Reconstruction, Midfoot Reconstruction, Hallux Valgus Reconstruction. Elbow. Wrist. Hand: Scapholunate Ligament Reconstruction, Ulnar Collateral Ligament Reconstruction, Radial Collateral Ligament Reconstruction, Biceps Tendon Reattachment. Knee: Extra Capsular Repairs - Medial Collateral Ligament, Lateral Collateral Ligament, Posterior Oblique Ligament, Illiotibial Band Tenodesis, Patellar Tendon Repair. Pelvis: Bladder Neck Suspension Procedures. Single patient use only

    Device Description

    The Surgicraft Screw Fixation System is manufactured from stainless steel and titanium. The self-tapping 3.5 mm screws are available in lengths from 20- 40 mm in 1 mm increments. The washers have an inner hole diameter of 4.2 mm and an outer diameter ranging from 7 to 9 mm in 1 mm increments.

    AI/ML Overview

    The provided text is a 510(k) Summary for the Surgicraft Screw Fixation System. It outlines the device description, intended use, and substantial equivalence to predicate devices, focusing on non-clinical mechanical testing. It does not contain information about acceptance criteria or a study that proves the device meets those criteria in the context of AI/algorithm performance.

    Therefore, I cannot populate the requested table and answer the specific questions related to AI/algorithm performance, ground truth, sample sizes for test/training sets, expert qualifications, or MRMC studies.

    The document states:

    • "Non-Clinical Testing: The Surgicraft Screw Fixation System was tested as follows: • Mechanical Testing ASTM - F543 - Standard Specification and Test Methods for Metallic Medical Bone Screws"
    • "Clinical Testing: Not applicable to this device"

    This means the device's performance was evaluated through mechanical testing against an ASTM standard, not a study involving AI or human interpretation of medical images/data. The absence of clinical testing further confirms this.

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