Vertebral Technologies, Inc.
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
SKU K091988UPC MAX
In Stock
—
IIFDA 510(k) Cleared (K091988)
1
Free shipping on orders over $99 · 30-day returns
Vertebral Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076 is an FDA 510(k)-cleared medical device (K091988) 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 July 29, 2009. Regulation: 8.
