Our kerrisons are available in hundreds of different configurations. See the possibilities on pages 6/2-6/15 of catalog #6.
The FDA reclassified spinal kerrisons and rongeurs as Class II devices, meaning that they now require 510(k) certification. Follow the below link to see the 510(k) certification for Fehling kerrisons and rongeurs.
See if our MI TLIF retractor (LVB-1) would be a welcome addition to your operating room!