K&J Consulting Corporation - FDA 510(k) Cleared Devices
Recent clearances: FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System, K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - K&J Consulting Corporation Orthopedic ✕
2 devices