Trans1 Incorporated
AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II
SKU K092124UPC KWQ
In Stock
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IIFDA 510(k) Cleared (K092124)
1
Free shipping on orders over $99 · 30-day returns
Trans1 Incorporated
Free shipping on orders over $99 · 30-day returns
AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II is an FDA 510(k)-cleared medical device (K092124) manufactured by Trans1 Incorporated. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 20, 2010. Regulation: 8.
