Recall Z-0605-2019 — Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and minimally invasive PLIF or TLIF surgical procedure.
U.S. FDA — Device Enforcement · United States · 2018-11-28 · Class II
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Reported risk: The surgical technique is being updated to caution against misuse due to reports of cage fractures occurring intra-operatively and post-operatively.
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