FDA 510(k) Applications Submitted by Alexandra Kirby

FDA 510(k) Number Submission Date Device Name Applicant
K210893 03/25/2021 Restoration Anatomic Shell Howmedica Osteonics Corp. a.k.a. Stryker Orthopaedics
K231469 05/22/2023 PAXgene« Blood DNA Tube PreAnalytiX GmbH
K223243 10/20/2022 BD Microtainer« Contact-Activated Lancets; BD Microtainer« QuikheelÖ Lancets Becton, Dickinson and Company
K193429 12/10/2019 Exeter V40 Femoral Stem, Exeter X3 RimFit Cup Howmedica Osteonics Corp


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