Precision Spine® Launches the Dakota ACDF™ Standalone System


2021-09-27 22:00:03 BioSpace


“With the inclusion of differentiating dual thread screws and high screw angulations, the Dakota ACDF system offers superior fixation and stability,” said Payam Farjoodi, MD from Coastline Orthopaedic Associates in Fountain Valley, CA. “The unsurpassed ease of use provided by the intuitive instrumentation makes it an ideal system for even the most challenging cases.” “The Dakota ACDF System represents another example of how Precision Spine is making good on its commitment to develop surgeon-designed devices that embody the advanced features surgeons need to help improve OR efficiency and achieve positive patient outcomes,” said Chris DeNicola, Chief Operating Officer of Precision Spine. The Dakota ACDF System is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C2-T1) at one-or two-disc levels with DDD defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies. The device is placed via an anterior approach at the C2 to T1 disc levels. Patients should have at least six weeks of non-operative treatment prior to treatment with an intervertebral fusion device such as the Dakota ACDF System. About Precision Spine Precision Spine, Inc. is a privately held company headquartered in Parsippany, NJ with manufacturing facilities in Pearl, MS. Precision Spine is dedicated to providing innovative, quality spine products that are made in the USA and designed to help treat serious orthopedic medical conditions in a cost-effective manner. For more information, visit View source version on Chris DeNicola Chief Operating Officer Source: Precision Spine, Inc. View this news release online at:
加利福尼亚州喷泉谷海岸线骨科协会的医学博士Payam Farjoodi说:“由于包括了差异化的双螺纹螺钉和高螺钉角度,Dakota ACDF系统提供了优越的固定和稳定性。”“直观的仪器提供的无与伦比的易用性使它成为一个理想的系统,即使是最具挑战性的情况。” “Dakota ACDF系统代表了精密脊柱如何兑现其承诺的另一个例子,即开发外科医生设计的设备,这些设备体现了外科医生需要的先进功能,以帮助提高或提高效率,并实现积极的病人结果,”精密脊柱首席运营官克里斯·德尼科拉说。 Dakota ACDF系统适用于一个或两个椎间盘水平的颈椎退行性椎间盘疾病(DDD)的骨骼成熟患者,DDD定义为椎间盘源性疼痛,并经病史和放射学检查证实椎间盘退行性病变。该装置通过前路放置在C2至T1椎间盘水平。患者在使用椎间融合器(如Dakota ACDF系统)治疗之前,应至少进行六周的非手术治疗。 关于精密脊柱 Precision Spine,Inc.是一家私人控股公司,总部位于新泽西州的Parsippany,生产设施位于Pearl。Precision Spine致力于提供创新、高质量的脊柱产品,这些产品在美国制造,旨在帮助以经济有效的方式治疗严重的骨科疾病。欲了解更多信息,请访问。 在businesswire.com查看源代码版本: 克里斯·德尼科拉 首席运营官 资料来源:Precision Spine,Inc. 在网上查看此新闻稿: