MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS

MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS is an FDA 510(k)-cleared medical device (K951846) manufactured by Alphatec Mfg., 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 February 13, 1996. Regulation: 8.