
Ionics Medical Corp.
Free shipping on orders over $99 · 30-day returns
DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K081673) manufactured by Ionics Medical Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 13, 2008. Regulation: 8.