Symmetry Sharp Kerrison Rongeur

Symmetry Sharp Kerrison Rongeur is an FDA 510(k)-cleared medical device (K161744) manufactured by Symmetry Surgical, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 6, 2016. Regulation: 8.