FDA 510(k) Applications Submitted by LESspine Innovations

FDA 510(k) Number Submission Date Device Name Applicant
K232605 08/28/2023 Sacrix« Sacroiliac Joint Fusion Device System, Inspan« ScrewLES Fusion System, Invue« MAXÖ + Invue Inset Anterior Cervical Plate System, and FacetFuse« Screw Fixation System LESspine Innovations


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