Spineology, Inc.
SPINEOLGY PEEK BULLET LUMBER INTERBODY FUSION DEVICE
SKU K111880UPC MAX
In Stock
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IIFDA 510(k) Cleared (K111880)
1
Free shipping on orders over $99 · 30-day returns
Spineology, Inc.
Free shipping on orders over $99 · 30-day returns
SPINEOLGY PEEK BULLET LUMBER INTERBODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K111880) 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 September 25, 2011. Regulation: 8.
