Vertebral Technologies, Inc.
INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
SKU K080673UPC MAX
In Stock
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IIFDA 510(k) Cleared (K080673)
1
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Vertebral Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K080673) manufactured by Vertebral Technologies, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 9, 2008. Regulation: 8.
