K&J Consulting Corporation FDA Approvals

0 new drug approvals and 2 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C Stand Alone System510(k)Dec 13, 2023	—	510(k)Substantially Equivalent (Traditional)	Dec 13, 2023
K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage510(k)Aug 27, 2021Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Aug 27, 2021