Captiva Spine, Inc.
PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)
SKU K092017UPC MAX
In Stock
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IIFDA 510(k) Cleared (K092017)
1
Free shipping on orders over $99 · 30-day returns
Captiva Spine, Inc.
Free shipping on orders over $99 · 30-day returns
PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD) is an FDA 510(k)-cleared medical device (K092017) manufactured by Captiva Spine, 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 November 30, 2009. Regulation: 8.
