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510(k) Data Aggregation

    K Number
    K210994
    Manufacturer
    Date Cleared
    2021-06-01

    (60 days)

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

    Arthrex Beveled FT Screws

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

    The Arthrex Beveled FT Screws are indicated for fixation of bone reconstruction. Examples include:

    • . Mono or Bi-Cortical osteotomies in the foot or hand
    • . Distal or Proximal metatarsal or metacarpal osteotomies
    • . Weil osteotomy
    • . Fusion of the first metatarsophalangeal joint and interphalangeal joint
    • . Fixation of osteotomies for Hallux Valgus treatment (such as Scarf, Chevron, etc.)
    • Akin type osteotomy
    • Arthrodesis base first metatarsal cuneiform joint to reposition and stabilize metatarsus varus primus .
    • . Calcaneus/cuboid arthrodesis
    • Talar/navicular arthrodesis
    Device Description

    The Arthrex Beveled FT Screws are fully threaded, cannulated screws with self-tapping, tapering head. The screws will be offered in three diameters: 3.5 mm, 4.0 mm and 4.5 mm, and will range in lengths from 12 mm to 60 mm. The screws are manufactured from Titanium Alloy, conforming to ASTM Standards F1472. The screws are sold sterile and non-sterile and are single use.

    AI/ML Overview

    This document is a 510(k) Premarket Notification from the FDA regarding the Arthrex Beveled FT Screws. It's a regulatory clearance document, not a study report for an AI/ML medical device. Therefore, it does not contain the information requested about acceptance criteria and study data for an AI/ML device.

    The "Performance Data" section describes mechanical and biological testing of the bone screws, confirming their physical properties, MRI compatibility, and biocompatibility, not performance of a software algorithm.

    To answer your request, I would need a document describing the regulatory clearance for an AI/ML medical device.

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