LDR Receives FDA Approval for Minimally Invasive Spinal Surgery Device

LDR has received 510(k) clearance from the FDA to market its Avenue L Lateral Lumber Cage System.

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Avenue L features enhanced in-line, self-guided VerteBRIDGE plating technology to facilitate simplified cage insertion and zero-profile, intradiscal, integrated fixation through a direct, minimally invasive approach. The Avenue L lateral cage has been used in Europe since 2010 with over 300 cases completed.

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