FDA 510(k) Applications Submitted by Vito Lore

FDA 510(k) Number Submission Date Device Name Applicant
K172484 08/17/2017 A-CIFT SoloFuse SpineFrontier, Inc.
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
K193106 11/08/2019 SpineFrontier Lumbar Interbody Fusion Device System SpineFrontier, Inc.


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