FDA 510(k) Applications Submitted by Daniela Mahan

FDA 510(k) Number Submission Date Device Name Applicant
K200956 04/09/2020 NuVasive Thoracolumbar Plates NuVasive, Incorporated
K201820 07/01/2020 NuVasive Thoracolumbar Interbody Systems: CoRoent Thoracolumbar System, CoRoent XL Interfixated System, Brigade Standalone System and Brigade Hyperlordotic System, Brigade Lateral System, BASE Interfixated Titanium System, Coalesce Thoracolumbar Interbody NuVasive, Incorporated
K222240 07/26/2022 EXPLORER AIR« II SurgVision GmbH
K214097 12/28/2021 Explorer Air II SurgVision GmbH


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