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FDA 510(k) Applications Submitted by Eminent Spine, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230219
01/26/2023
Eminent Spine 3D Lumbar Interbody Fusion Systems
Eminent Spine, LLC
K201979
07/16/2020
Cervical Plate System
Eminent Spine, LLC
K212853
09/07/2021
Cervical Stand-Alone System
Eminent Spine, LLC
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