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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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