FDA clears Nvision's 3D printed PEEK Interbody System made using Invibio's PEEK-OPTIMA and Bond3D additive manufacturing ...

Cerapedics Inc., a global, commercial-stage orthopedics company dedicated to redefining the standard of care for bone repair, today announced the U.S. Food and Drug Administration (FDA) approval for ...

Spineology Inc., today unveiled a new brand and visual identity, logo, and product positioning as part of an extensive ...

The North American Spine Society is a global multidisciplinary medical society that utilizes education, research, and advocacy to foster the highest quality, ethical, and evidence-based spine care.

According to Spine Wave, the all-titanium implant features simple and easy to use instruments and a biplanar taper for easier ...

Back pain is a common ailment affecting millions worldwide, often disrupting daily life and productivity. For many, the pain ...

A study from Life Spine found that the company's endoscopic transforaminal lumbar interbody fusion platform performed as well as a minimally invasive tubular ap ...

The evidence of this updated meta-analysis indicated that PLIF results in a higher complication rate than does TLIF, based on 7 high methodological quality studies of epidemiological data. PLIF ...

Objectives: Minimally invasive transforaminal lumbar interbody fusion (Mis-TLIF) and oblique lumbar interbody fusion (OLIF) are increasingly replacing traditional approaches. This study aimed to ...

This site displays a prototype of a “Web 2.0” version of the daily Federal Register. It is not an official legal edition of the Federal Register, and does not replace the official print version or the ...

21. 1. SI-Bone earned FDA 510(k) clearance and breakthrough device designation for the iFuse Torq TNT implant system. 2. Globus Medical launched the Adira extreme lateral interbody fusion plate system ...