Ldr Spine USA
LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM
SKU K070341UPC KWP
In Stock
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IIFDA 510(k) Cleared (K070341)
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Free shipping on orders over $99 · 30-day returns
Ldr Spine USA
Free shipping on orders over $99 · 30-day returns
LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM is an FDA 510(k)-cleared medical device (K070341) manufactured by Ldr Spine USA. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 7, 2007. Regulation: 8.
