Spinal USA
SPINAL USA INTERBODY FUSION DEVICE
SKU K080314UPC MAX
In Stock
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IIFDA 510(k) Cleared (K080314)
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Free shipping on orders over $99 · 30-day returns
Spinal USA
Free shipping on orders over $99 · 30-day returns
SPINAL USA INTERBODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K080314) manufactured by Spinal USA. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 12, 2008. Regulation: 8.
