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K&J Consulting Corporation

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K232877 FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone SystemMRW2023-12-13 View
510(k) K212038 K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK CageODP2021-08-27 View
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