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Aurora Spine Announces Initial Surgeries Conducted Using its SiLO TFX™ MIS Sacroiliac Joint Fixation System

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Aurora Spine Corporation (OTCQB: ASAPF) announced the successful initial surgeries of its FDA-approved SiLO TFX™ MIS Sacroiliac Joint Fixation Device, with over a dozen patients receiving the implant. The SiLO TFX is designed for sacroiliac joint fusion, targeting conditions like joint disruptions and degenerative sacroiliitis. With a significant market potential, 30 million Americans suffer from lower back pain, with 4.7 million experiencing SI joint pain. The device simplifies the implantation process, aligning with existing non-surgical treatment methods. CEO Trent Northcutt expressed optimism regarding the device's capability to enhance surgical outcomes, signaling a forthcoming full market launch by mid-year. Surgeons have praised the device's seamless technique and potential for superior results.

Positive
  • Successful initial surgeries of SiLO TFX performed on over a dozen patients.
  • FDA-approved device targeting a significant market of 4.7 million SI joint pain patients.
  • $2.3 billion market opportunity for SI joint fixation surgical procedures annually.
  • Device designed for ease of use, aligning with existing non-surgical treatment practices.
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  • None.

Carlsbad, Calif., April 17, 2023 (GLOBE NEWSWIRE) -- Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV:ASG) (OTCQB: ASAPF), a designer and manufacturer of innovative medical devices that improve spinal surgery outcomes, today announced that initial surgeries using its proprietary SiLO TFX™ MIS Sacroiliac Joint Fixation Device have been performed in recent weeks. Over a dozen patients were implanted with the newly FDA-approved device and all procedures using the device were successful.

The patented, minimally invasive SiLO TFX MIS Sacroiliac Joint Fixation System is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis. The SiLO TFX MIS Sacroiliac Joint Fixation System includes a Transfixing-Cone, an ilium screw, a sacrum screw and associated instrumentation. The SiLO TFX implants are designed to transfix the sacrum and ilium, providing stability for bony fusion.

The market opportunity for the SiLO TFX is sizable, as over 30 million people suffer from lower back pain in the U.S. alone, of which, approximately 4.7 million are SI joint pain patients and treated with non-surgical treatments. One treatment are therapeutic injections, of which there are 1.2 million administered per year. The SiLO TFX was designed for ease of implantation and uses similar approach of the injection, making the implantation seamless for doctors that already know how to administer an injection in the SI join. Longer-term suffers of SI joint pain now have minimally invasive surgical options, including the SiLO TFX, of which approximate in excess of 250,000 cases per year or more than $2.3 billion market opportunity per year in the U.S. alone.

Mr. Trent Northcutt, Aurora’s President, CEO and co-founder, stated, "We are pleased with these initial surgeries using our SiLO TFX, which is a game changing device for the industry. These surgeries will enable us to enter into the next phase of commercialization, whereby we’ve begun to build inventory and kits to gear up for a full launch of the product by mid-year.”

Dr. Michael Stoffman, Neurosurgeon at the University at Buffalo Neurosurgery, said “SiLo TFX is a seamless, precise and efficient method to safely transfix the SI joint. I believe the SiLO TFX will result in superior clinical outcomes based on our positive biomechanical data with head to head testing of other transfixing SI joint devices.”

Dr. Steven Falowski, a Functional Neurosurgeon in Lancaster, PA, commented, “The SiLO TFX marks the next chapter in treating patients safely and effectively with a minimally invasive option for sacroiliac joint fixation. It incorporates two well-known techniques of graft placement into the joint, and transfixation across the sacrum and ilium. The instrumentation allows for a smooth placement with a single small incision improving both the physician and patient experience."

About Aurora Spine

Aurora Spine is focused on bringing new solutions to the spinal implant market through a series of innovative, minimally invasive, regenerative spinal implant technologies. Additional information can be accessed at www.aurora-spine.com or www.aurorapaincare.com.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

Forward-Looking Statements

This news release contains forward-looking information that involves substantial known and unknown risks and uncertainties, most of which are beyond the control of Aurora Spine, including, without limitation, those listed under "Risk Factors" and "Cautionary Statement Regarding Forward-Looking Information" in Aurora Spine's final prospectus (collectively, "forward-looking information"). Forward-looking information in this news release includes information concerning the proposed use and success of the company’s products in surgical procedures. Aurora Spine cautions investors of Aurora Spine's securities about important factors that could cause Aurora Spine's actual results to differ materially from those projected in any forward-looking statements included in this news release. Any statements that express, or involve discussions as to, expectations, beliefs, plans, objectives, assumptions or future events or performance are not historical facts and may be forward-looking and may involve estimates, assumptions and uncertainties which could cause actual results or outcomes to differ unilaterally from those expressed in such forward-looking statements. No assurance can be given that the expectations set out herein will prove to be correct and, accordingly, prospective investors should not place undue reliance on these forward-looking statements. These statements speak only as of the date of this press release and Aurora Spine does not assume any obligation to update or revise them to reflect new events or circumstances.

Contact:

Aurora Spine Corporation

Trent Northcutt

President and Chief Executive Officer

(760) 424-2004

Chad Clouse

Chief Financial Officer

(760) 424-2004

www.aurora-spine.com

Adam Lowensteiner

LYTHAM PARTNERS, LLC

Phoenix | New York

Telephone: 646-829-9700

asapf@lythampartners.com


FAQ

What is the SiLO TFX device from Aurora Spine?

The SiLO TFX is a minimally invasive sacroiliac joint fixation device aimed at improving spinal surgery outcomes.

When was the SiLO TFX device launched?

Initial surgeries using the SiLO TFX device were performed recently, with a full market launch expected by mid-year 2023.

What conditions does the SiLO TFX target?

The device is intended for sacroiliac joint fusion for conditions like sacroiliac joint disruptions and degenerative sacroiliitis.

What is the market opportunity for the SiLO TFX?

The device addresses a market need for over 4.7 million SI joint pain patients in the U.S., potentially exceeding $2.3 billion annually.

Who commented on the device's effectiveness?

Neurosurgeons including Dr. Michael Stoffman and Dr. Steven Falowski have praised the SiLO TFX for its precision and efficiency.

AURORA SPINE CORP

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