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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