Kalitec Direct, LLC
INTESS LUMBAR CAGE
SKU K123100UPC MAX
In Stock
—
IIFDA 510(k) Cleared (K123100)
1
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Kalitec Direct, LLC
Free shipping on orders over $99 · 30-day returns
INTESS LUMBAR CAGE is an FDA 510(k)-cleared medical device (K123100) manufactured by Kalitec Direct, 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 March 27, 2013. Regulation: 8.
