K&J Consulting Corporation

K&J Consulting Corporation holds 2 FDA 510(k) medical device clearances, first cleared 2021, most recent 2023.

Top product codes for K&J Consulting Corporation

MRW — Unknown1 device
ODP — Orthopedic1 device

Recent clearances by K&J Consulting Corporation

K232877 — FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C Stand Alone SystemCode MRW·2023-12-13
K212038 — K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK CageCode ODP·2021-08-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.