
Ldr Spine USA, Inc.
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LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS is an FDA 510(k)-cleared medical device (K113559) 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 December 28, 2011. Regulation: 8.