三友医疗(688085.SH)金属增材制造椎间融合器系列产品获美国FDA510(K)认证

智通财经2023-12-14

智通财经APP讯，三友医疗(688085.SH)公告，公司近日收到 U.S. Food and Drug Administration(美国食品药品监督管理局，“FDA”)的通知，公司金属增材制造椎间融合器系列产品获得美国 FDA 510(K)认证。据悉，金属增材制造椎间融合器系列产品与脊柱内固定产品配合使用，适用于患有退行性椎间盘疾病的骨骼成熟的患者。有以下适应症：退行性椎间盘疾病(定义为背痛...

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