FDA 510(k) Applications Submitted by K&J Consulting Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K212038 06/30/2021 K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage K&J Consulting Corporation
K232877 09/15/2023 FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-CÖ Stand Alone System K&J Consulting Corporation


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