Lanx, LLC
LANX INTERVERTEBRAL BODY FUSION DEVICE
SKU K073144UPC MAX
In Stock
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IIFDA 510(k) Cleared (K073144)
1
Free shipping on orders over $99 · 30-day returns
Lanx, LLC
Free shipping on orders over $99 · 30-day returns
LANX INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K073144) manufactured by Lanx, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 23, 2008. Regulation: 8.
