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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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