Spinal Tech

DeGen Medical recently received FDA clearance for its F1 MPS modular pedicle screw system for the Joust minimally invasive procedure.

The FDA recently granted 510(k) clearance for Life Spine's Hinged laminoplasty system.

Brainlab launched Loop-X, its mobile intraoperative imaging robot, at the North American Spine Society Annual Meeting in Chicago on Sept. 25.

Abbott received FDA approval for Proclaim XR, a neurostimulation device for people suffering from chronic pain.

The Spine Journal published the results of Stryker's SAKOS pivotal trial for the SpineJack implantable fracture reduction system.

Medical device distributor OM Surgical Solutions expanded its portfolio of physician support resources by acquiring Docs Dial, a medical marketing company.

Disruptive medical device companies are shaking up the status quo in orthopedics, according to OrthoStreams.

Medtronic has received FDA approval to move forward with a prospective, randomized pivotal clinical trial that will examine the use of Infuse in transforaminal lumbar interbody fusions. 

Lower back pain (LBP) is one of the most prevalent musculoskeletal conditions and a significant public health burden.1 Clinical publications have identified the SI joint as a pain generator in 15-30% of chronic LBP patients.2–6 The prevalence of SI joint pain in symptomatic post-lumbar…

Life Spine announced on Sept. 24 that the initial surgeries performed with the ProLift Lateral Expandable Spacer System.