FDA 510(k) Applications Submitted by Stephen Courtney

FDA 510(k) Number Submission Date Device Name Applicant
K230219 01/26/2023 Eminent Spine 3D Lumbar Interbody Fusion Systems Eminent Spine, LLC
K240505 02/21/2024 Eminent Spine SI Screw System Eminent Spine, LLC
K241663 06/07/2024 Eminent Spine 3D Titanium Pedicle Screw System Eminent Spine
K221936 07/01/2022 Standalone ALIF Interbody Fusion System Eminent Spine
K242069 07/15/2024 Eminent Spine Scoliosis Deformity Pedicle Screw System Eminent Spine
K201979 07/16/2020 Cervical Plate System Eminent Spine, LLC
K212701 08/25/2021 Eminent Spine 3D Cervical Interbody Fusion System Eminent Spine
K212853 09/07/2021 Cervical Stand-Alone System Eminent Spine, LLC


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