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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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