Ldr Spine USA, Inc.
LDR SPINE USA AVENUE L INTERBODY FUSION
SKU K113285UPC OVD
In Stock
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IIFDA 510(k) Cleared (K113285)
1
Free shipping on orders over $99 · 30-day returns
Ldr Spine USA, Inc.
Free shipping on orders over $99 · 30-day returns
LDR SPINE USA AVENUE L INTERBODY FUSION is an FDA 510(k)-cleared medical device (K113285) manufactured by Ldr Spine USA, 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 July 25, 2012. Regulation: 8.
