Medical Device News Magazine

Orthofix Medical Expands Synthetic Bone Growth Offerings with Full Market Launch of Opus BA – a Bioactive Solution for Spine Procedures

About Medical Device News Magazine

About Medical Device News Magazine. We are a digital publication founded in 2008 located in the United States.

Advertise with Medical Device News Magazine! Join Our #1 Family of Advertisers!

We pride ourselves on being the best-kept secret when it comes to distributing your news! Our unique digital approach enables us to circulate your...

Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and orthopedics focus, today announced the full market launch of Opus BA, a synthetic bioactive bone graft solution for cervical and lumbar spine fusion procedures.

Available in putty and strip formulations, Opus BA can be used to fill bone voids or gaps in the skeletal system that are not intrinsic to the stability of bony structure. Opus BA acts as a scaffold allowing bone growth across the surface that is reabsorbed and replaced with natural bone during the healing process. Easily hydrated with autogenous bone marrow or autograft with saline, Opus BA is moldable and ideal for versatile applications.

“Bioactive synthetics are a very large and growing market,” said President of Orthofix Global Spine Kevin Kenny. “We recognize that each bone substitute has its own unique advantages and surgeons have different preferences when evaluating the use of autologous, allogeneic or synthetic bone graft materials for their patients. The addition of Opus BA is another example of our commitment to providing surgeons with a wide range of solutions so they can select the best bone substitute for each patient.”

Opus BA’s osteoconductive matrix is made up of a carefully selected mix of components: carbonate apatite bone mineral, bioactive glass, and Type 1 Collagen carrier. These materials were selected for the ability to stimulate the growth, formation and resorption of bone. Opus BA undergoes a proprietary process to ensure the osteoconductive matrix has uniform distribution, mimicking the structure and porosity of cancellous bone.

Orthofix invites those attending the Congress of Neurological Surgeons Spine Summit 2022 Annual Meeting in Las Vegas, Nevada, February 24-25, 2022 to visit booth #212 to learn more about the Orthofix family of products. The latest data on Opus BA will be presented in a sponsored session entitled “The Clinical Value of Bioactive Synthetics in Spine Surgery” on February 25.

Orthofix recognizes the important role of a comprehensive offering of biologic solutions in spine and orthopedic surgical applications. The Company proudly markets and distributes the Trinity Elite and Trinity Evolution allografts with viable cells, FiberFuse Advanced moldable allograft, FiberFuse Strip preformed allograft, AlloQuent structural allograft, VersaShield amniotic membrane, Opus Mg Set bone void filler, Collage osteoconductive scaffold, and the O-Genesis graft delivery system. This broad portfolio gives surgeons the ability to select the best option to meet their procedural and patient needs.

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Other News

Shoulder Innovations Further Strengthens IP Portfolio in Key Areas with Recent Patent Grants

"These recent grants further strengthen key patent families that are foundational to our technology, and we are pleased the USPTO continues to recognize our meaningful innovation in the shoulder arthroplasty segment," said Rob Ball, CEO of Shoulder Innovations. "This noteworthy expansion of our IP position represents the culmination of over 10 years of research and development, and we are proud of our team for their continued dedication to creating practical solutions for shoulder surgeons and advancing patient outcomes."

Radical Catheter Technologies Presents Analysis of Disruptive, Recently FDA-Cleared Endovascular Technology at the Society of NeuroInterventional Surgery 21st Annual Meeting

This new catheter, the first product commercialized from this novel technology platform, is designed to enable access to the blood vessels in the brain for both femoral and radial access. A multi-center analysis of this disruptive technology is being presented today at Society of NeuroInterventional Surgery 21st annual meeting. In addition, the Company confirmed the closing of a $20 million financing round led by NeuroTechnology Investors, which will be used to scale the company and expand the Radical platform notes Radical Catheter Technologies.

Rapid Medical™ Completes Initial Neurovascular Cases in the USA Following FDA Clearance of Its Active Access Solution

“With DRIVEWIRE, our design goal was to bring new levels of access and control to the interventional suite while improving best-in-class guidewires,” comments Giora Kornblau, Chief Technology Officer at Rapid Medical. “When physicians are looking for technologies that increase the clinical possibilities and safety for the patient, we want Rapid to be the first place they look.”