Alphatec Spine, Inc.
GUIDED LATERAL INTERBODY FUSION (GLIF) SYSTEM
SKU K090425UPC MAX
In Stock
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IIFDA 510(k) Cleared (K090425)
1
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Alphatec Spine, Inc.
Free shipping on orders over $99 · 30-day returns
GUIDED LATERAL INTERBODY FUSION (GLIF) SYSTEM is an FDA 510(k)-cleared medical device (K090425) manufactured by Alphatec 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 May 18, 2009. Regulation: 8.
