Spineology, Inc.
SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE
SKU K123652UPC MAX
In Stock
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IIFDA 510(k) Cleared (K123652)
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Free shipping on orders over $99 · 30-day returns
Spineology, Inc.
Free shipping on orders over $99 · 30-day returns
SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K123652) manufactured by Spineology, 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 March 21, 2013. Regulation: 8.
