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510(k) Data Aggregation

    K Number
    K023862
    Manufacturer
    Date Cleared
    2002-12-19

    (29 days)

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

    NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER

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

    Norian® XR Calcium Phosphate Bone Void Filler is intended only for bony voids or defects that are not intrinsic to the stability of the bony structure. Norian® XR Calcium Phosphate Bone Void Filler is intended to be placed or injected into bony voids or gaps of the skeletal system (i.e., the extremities, spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs over a period of years and is replaced with bone during the healing process.

    Device Description

    Norian® XR, USP is an injectable, moldable, biocompatible bone void filler. The reactants pack contains sterile powder (calcium phosphate) with BaSO4 added for radiopacity and solution (dilute sodium phosphate). The Reactants Pack is designed to be placed in a reusable mixer where the components are mixed together to form a smooth, viscous paste that remains injectable for approximately 5 minutes at 18-23°C. Norian® XR begins to harden after 2 minutes and sets in approximately 10 minutes at body temperature (37°C). Norian® XR is slowly resorbed over a period of years. The 3cc, 5cc, 7.5cc, and 10cc Reactants Packs are provided sterile and are for single use only.

    AI/ML Overview

    I am sorry, but the provided text focuses on the regulatory approval of a medical device (Norian® XR Calcium Phosphate Bone Void Filler) and does not contain information about acceptance criteria or a study proving that the device meets such criteria. The document is a 510(k) summary and approval letter from the FDA, which confirms the device's substantial equivalence to previously marketed devices. It does not detail specific performance metrics, clinical study designs with test sets, ground truth establishment, or expert evaluations.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the provided text.

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