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

FDA 510(k) Number Submission Date Device Name Applicant
K231460 05/19/2023 FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, BALTEUMÖ & BALTEUM-ONEÖ Lumbar Plate System, and OspreyÖ Anterior Cervical Plate System K&J Consulting Corp.
K232586 08/25/2023 Rexious Spinal Fixation System, StateraÖ Spinal System, Statera-MÖ Spinal System K&J Consulting Corp.
K233332 09/29/2023 Statera-CÖ Spinal System K&J Consulting Corp.


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