Medical Device News

Precision Spine Launches Reform MC (Midline Cortical) System

Designed to Reduce Muscle Disruption

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...

Today Precision Spine, Inc. (a medical device company dedicated to Made-in-the-USA manufacturing) announced the launch of the Reform® MC (Midline Cortical) System, which utilizes a minimally disruptive approach designed to reduce muscle retraction laterally past the facet joint, and requires a smaller incision while maintaining direct visualization and access to the disc space.

The Reform MC system is a top-loading, multiple component, posterior spinal fixation system which consists of cannulated pedicle screws, straight and lordotic rods, and locking cap screws. Components are available in a variety of sizes to closely match patient anatomy.

“I have found that the Reform MC system’s medial to lateral trajectory, combined with its distinctive cortical cancellous screw thread design, helps achieve greater cortical bone purchase,” said Nicholas Renaldo, M.D. “Its modular screw design maximizes visualization and its low-profile, 4.75mm diameter cobalt chrome tulip helps conserve space without compromising strength.”

The Reform MC System is modular to enable intraoperative flexibility and confidence, featuring multiple size tulips, audible attachment, consistent assembly force, and a T25 drive feature. A tri-zone cortical-cancellous thread form with a stepped proximal diameter and an aggressive quick-start tip optimizes bone purchase during final seating. The system’s retractor delivers optimal access while minimizing muscle disruption, with 30° articulating arms and integrated dual fiber optics, and easy snap-on anatomically contoured, radiolucent blades in multiple length options increase procedure flexibility.

“The Reform MC System is an important step forward in the expansion of our Reform family of devices as we continue working with surgeons to design and commercialize advancements that combine versatility, efficiency, and cost-effectiveness,” said Chris DeNicola, Chief Operating Officer of Precision Spine.

The system is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion (pseudarthrosis). It is also indicated for pedicle screw fixation for the treatment of severe spondylolisthesis (Grades 3 and 4) of the L5-S1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum) with the removal of the implants after the attainment of a solid fusion. The system is also intended for non-cervical pedicle screw fixation (T1-S1/ilium) for the following indications: degenerative disc disease (as defined by back pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies); trauma (i.e. fracture or dislocation); spinal stenosis; curvatures (i.e. scoliosis, kyphosis; and/or lordosis); spinal tumor; pseudarthrosis; and failed previous fusion. When used for posterior non-cervical pedicle screw fixation in pediatric patients, the Reform Pedicle Screw System is indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis. The Reform Pedicle Screw System is intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach.

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

Ultrahuman Announces its App Store ‘PowerPlugs’ with the World’s First AFib Detection Technology on a Smart Ring

Recognizing each individual’s health journey is unique, PowerPlugs enable people to choose and focus on the aspects of their health that matter most. It’s designed for highly personalized health insights, ensuring that every individual can personalize their health tracking to their unique needs and goals.

VisionAir Solutions Celebrates Milestone and New Collaboration

This achievement marks VisionAir Solutions commitment to bringing technological innovation to pulmonary medicine. Since its acquisition by Theken Companies last year, VAS has over doubled its growth and continues to demonstrate industry adoption and the advantages of personalized healthcare.

Valencia Technologies Announces CMS Publication of 2025 Medicare Proposed Rule for eCoin® Procedure

Ann Decker, VP of Reimbursement for Valencia Technologies, stated, "The cumulative effect of the proposed 2025 continuation of APC assignment 5464, the improved ASC payment rate, and the recognition of ITNS as a minimally invasive OAB treatment option in the recently updated guidelines by the American Urological Association (AUA) and the Society of Urodynamics, Female Pelvic Medicine, and Urogenital Reconstruction (SUFU), underscores that the eCoin ITNS system will have a strong reimbursement pathway throughout 2025 and beyond.