Raymond J. Linovitz

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STUDY DESIGN A prospective, randomized, multicenter, Food and Drug Administration-regulated Investigational Device Exemption clinical trial. OBJECTIVE To evaluate the safety and effectiveness of(More)
This multicenter clinical study was performed to assess the safety and effectiveness of Trinity Evolution® (TE), a viable cellular bone allograft, in combination with a PEEK interbody spacer and(More)
BACKGROUND Cellular bone allograft (CBA) possesses osteogenic, osteoinductive, and osteoconductive elements essential for bone healing. The purpose of this study was to assess the safety and(More)
BACKGROUND CONTEXT The most commonly used materials used for interbody cages are titanium metal and polymer polyetheretherketone (PEEK). Both of these materials have demonstrated good(More)
BACKGROUND Trinity Evolution® (TE), a viable cellular bone allograft, previously demonstrated high fusion rates and no safety-related concerns after single-level anterior cervical discectomy and(More)
BACKGROUND Trinity Evolution® cellular bone allograft (TE) possesses the osteogenic, osteoinductive, and osteoconductive elements essential for bone healing. The purpose of this study is to evaluate(More)
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