Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Wenzel Spine
Free shipping on orders over $99 · 30-day returns
WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM is an FDA 510(k)-cleared medical device (K100820) manufactured by Wenzel Spine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 2010. Regulation: 8.