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510(k) Data Aggregation

    K Number
    K091614
    Manufacturer
    Date Cleared
    2009-09-10

    (99 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    OSTEOMED FOOT PLATING SYSTEM

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

    The OsteoMed Foot Plating System is indicated for use in trauma, general surgery, and reconstructive procedures of the foot, ankle or other bones appropriate for the device.

    The OsteoMed Foot Plating System implants are intended for single use only.

    Device Description

    This submission describes the OsteoMed Foot Plating System consisting of various shape and sizes plates featuring compression, locking, elongated or compression elongated holes, and ulated locking, non-locking and cannulated screws, implantable K-wires, washers, and angulated instrumentation. The OsteoMed Foot Plating System is indicated for use in trauma, general surgery, and reconstructive procedures of the foot, ankle or other bones appropriate for the size of the device. All implants are intended for single use only. Surgical instrumentation is provided to facilitate modification, insertion, and removal of implants.

    The system contains several modules based on the size of the device and application site such as fixation/reconstruction of small fragment bones, forefoot, mid-foot, rear-foot, ankle, , or other bones appropriate for the size of the device.

    The implants are made of Titanium (ASTM F-67, ASTM F-136, or ASTM F-1472) or Stainless Steel (ASTM F-138 or ASTM F-139). The instrumentation is made from various grades of stainless steel, anodized aluminum, and/or medical grade polymers.

    AI/ML Overview

    The provided text does not contain information about acceptance criteria or a study proving that the OsteoMed Foot Plate and Screw Rigid Fixation System meets such criteria. The document is a 510(k) premarket notification summary and an FDA clearance letter. It focuses on establishing substantial equivalence to predicate devices based on similarities in intended use, materials, design, and operational principles.

    Therefore, I cannot provide the requested table, sample sizes, expert details, adjudication methods, MRMC study information, standalone performance, or ground truth details.

    The document explicitly states: "Due to the similarity of materials and design to both pre-enactment and post-enactment devices we believe that the OsteoMed Foot Plating System does not raise any new safety or effectiveness issues." This statement suggests that the clearance was based on demonstrating equivalence to existing, legally marketed devices rather than on a new performance study with specific acceptance criteria as you've outlined.

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