Spine News

Results showed a postoperative pain management protocol with liposomal bupivacaine decreased opioids and length of stay and improved ambulation in patients with adolescent idiopathic scoliosis who underwent posterior spinal fusion.

LAS VEGAS — Results presented here showed anterior decompression and fusion via a posterolateral approach may be safe and effective for treatment of beak-type ossification of the posterior longitudinal ligament in the thoracic spine.

A potential new treatment for early onset scoliosis, the Spring Distraction System by Cresco Spine, has received a breakthrough device designation from the FDA, according to a company press release.

Healio celebrates Mental Health Awareness Month with a focus on physician burnout, an emerging public health crisis among orthopedic physicians and providers.

VySpine has announced FDA 510(k) clearance of its UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion system, according to a press release.

Proprio has announced FDA 510(k) clearance of its Paradigm spine surgery navigation platform, according to a company press release.

Implanet has announced FDA 510(k) clearance of its Squale anterior cervical cage, according to a company press release.

Published results showed a prehabilitation intervention program was associated with improved preoperative and postoperative outcomes for patients undergoing orthopedic surgery.

The FDA issued a final rule to classify spinal spheres for use in intervertebral fusion procedures into class III assignment and to require the filing of premarket approval applications for these products.

Synapse Biomedical has received premarket approval from the FDA for its NeuRx Diaphragm Pacing System, which aids adults with spinal cord injuries that require ventilation to breathe, according to a company press release.