Vertebral Technologies, Inc.
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
SKU K102277UPC MAX
In Stock
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IIFDA 510(k) Cleared (K102277)
1
Free shipping on orders over $99 · 30-day returns
Vertebral Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K102277) 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 October 5, 2010. Regulation: 8.
