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510(k) Data Aggregation

    K Number
    K051656
    Date Cleared
    2005-10-25

    (126 days)

    Product Code
    Regulation Number
    888.1100
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    OCT (OSTEOCHONDRAL TRANSPLANT) COMPREHENSIVE SYSTEM

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

    The OCT (Osteochondral Transplant) Comprehensive System is indicated for arthroscopic (Knee and Ankle) and open osteochondral grafting for the treatment of osteochondral (cartilage) defects.

    Device Description

    The OCT (Osteochondral Transplant) Comprehensive System is a kit composed of several orthopedic surgical instruments. These instruments include Drill Sleeve Cap, Drills, Toothed Core Sleeve and Plunger, Obturators, Sizers, Drill Handle, Ruler and Drill Sleeves and Sterilization Tray. All instruments are composed of stainless steel and/or injection molded plastic. The instruments range in size from 3 to 11 mm.

    AI/ML Overview

    This appears to be a 510(k) premarket notification for a medical device (OCT Comprehensive System) and not a study describing the device's performance against acceptance criteria. There is no information in the provided text about acceptance criteria or a study proving the device meets them.

    The document is a communication from the FDA to OsteoBiologics, Inc., confirming that their device, the OCT (Osteochondral Transplant) Comprehensive System, is substantially equivalent to a previously cleared predicate device (Acufex "MosaicPlasty" Comprehensive System, K964215). This "substantial equivalence" determination is the basis for its clearance, not a performance study against specific acceptance criteria.

    Therefore, I cannot provide the requested information because it is not present in the provided text.

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