Life Spine
MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR
SKU K061698UPC JDK
In Stock
—
IIFDA 510(k) Cleared (K061698)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Life Spine
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR is an FDA 510(k)-cleared medical device (K061698) manufactured by Life Spine. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 11, 2006. Regulation: 8.
