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Astura Medical Receives FDA 510(k) Clearance For Dolomite Stand-Alone Anterior Cervical Stabilization System

November 9, 2020 By SPINEMarketGroup

IRVING, TX – November 9, 2020 – Astura Medical, a high-growth, innovative spine technology company, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Dolomite Stand-Alone Anterior Cervical Stabilization System.

Expanding on the rapid adoption and recent success of the company’s other integrated plate and spacer technologies for anterior lumbar and lateral lumbar procedures, Dolomite was designed to deliver the widest array of construct options with the most efficient and streamlined supporting instrumentation in the anterior cervical surgery marketplace today.

“Even in market segments that are well established and relatively commoditized, we are continuing to find ways to improve from other currently available technology,” said Joel Gambrell, Co-founder and
CEO. “Dolomite is yet another example of our R&D Team, alongside our surgeon design partners, reestablishing the benchmark of what is considered to be the best-in-class solution for a specific procedure.”

Dolomite provides the choice of either HA PEEK or Acid-etched Titanium interbody spacers in an extensive range of heights, widths, and lordotic options. The system provides the intraoperative flexibility to select between either a zero-profile, half plate, or full plate that can be implanted in conjunction with the interbody. By providing either anchoring nails or screws, which can be delivered via multiple techniques including an “All-in-One” option, Dolomite provides a streamlined, repeatable set of solutions that can accommodate the varying anatomical challenges presented in anterior cervical surgery.

Dolomite is the company’s third technology platform providing a combined interbody and fixation option to receive 510k approval within the last 6 months.

For more information on Dolomite, click here.

About Astura Medical

Astura Medical was formed in 2014 with the objective of creating a disciplined, multi-phased approach to developing, manufacturing, and distributing medical devices. With surgeon input and feedback at
every stage of development, Astura has created an extensive line of devices of the highest quality and sleekest design.

The two essential pillars that contribute to Astura Medical’s success are high quality products and robust distribution channels. These pillars, combined with passion and innovation, are what drive the Astura team to achieve great success with developing devices and entering them into the marketplace. For more information, please visit www.asturamedical.com or find us on LinkedIn.

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Media Contact:
Steve Haayen
Astura Medical
858.472.8825 [email protected]

(Visited 64 times, 12 visits today)

Filed Under: FDA, NEWS Tagged With: 2020, NEWS

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