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510(k) Data Aggregation

    K Number
    K190956
    Device Name
    SCS 17-01
    Date Cleared
    2020-01-30

    (294 days)

    Product Code
    Regulation Number
    888.3045
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Reference Devices :

    Stryker Hydroset (K161447)

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

    SCS 17-01 is a syntheic, biocompatible bone graft substitute material that hardens and converts to a poorly crystalline hydroxyapatite at body temperature. It is indicated for filling bone voids or defects of the skeletal system (i.e. extremites and pelvis) that are not intrinsic to the stability of bony structure. These defects may be surgically created osseous defects or defects created from traumatic injury to the bone. The device provides an injectable, self-setting, osteoconductive bone graft substitute that resorbs and is replaced by the growth of new bone during the healing process.

    Device Description

    The SCS 17-01 product is a synthetic, injectable, settable osteoconductive calcium phosphate bone graft substitute material. SCS 17-01 is composed of a dry powder and an aqueous solution (supplied in separate sterile, preloaded syringes) that must be mixed intra-operatively to form a cohesive paste prior to implantation using the supplied mixing system. The dry powder is composed of the alpha phase of tricalcium phosphate (alphaTCP) [Ca3(PO4)2], calcium [CaCO3] carbonate phosphate [Ca(H2PO4)2]. The aqueous component is composed of water for injection, sodium phosphate dibasic [Na2HPO4], citric acid [C6H8O7] and hyaluronic acid (HA). Upon mixing the cement powder and the setting solution at body temperature, a dissolution and reprecipitation reaction occurs resulting in the precipitation of a poorly crystalline hydroxyapatite. During the healing process, the bone void filler resorbs and is replaced with new bone growth. SCS 17-01 is provided sterile for single use in volumes ranging from 1cc to 4cc.

    AI/ML Overview

    I am sorry, but the provided text does not contain information about the acceptance criteria and a study proving a device meets these criteria in the context of an AI/ML powered medical device. The document is a 510(k) clearance letter for a bone void filler and describes its substantial equivalence to a predicate device based on bench tests, chemical and physical characterization, and an in vivo animal study. It does not refer to an AI device or any associated performance metrics or studies as described in your request.

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