NUVASIVE GUIDED SPINAL ARTHROSCOPY SYSTEM

NUVASIVE GUIDED SPINAL ARTHROSCOPY SYSTEM is an FDA 510(k)-cleared medical device (K990324) manufactured by Nuvasive, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 4, 1999. Regulation: 8.