
Ldr Spine USA, Inc.
Free shipping on orders over $99 · 30-day returns
LDR SPINE SPINETUNE TL SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K120760) manufactured by Ldr Spine USA, 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 June 26, 2012. Regulation: 8.