MACON, Ga.--(BUSINESS WIRE)--Southern Spine, LLC, an ISO 13485:2003 certified manufacturer of implants and instruments for spinal surgery, announced today the release of a current literature review on ...

SALT LAKE CITY--(BUSINESS WIRE)--Nexus Spine, a developer of biomechanically-advanced solutions for spinal pathologies, today announced the full commercial launch of its PressON™ posterior lumbar ...

Less than a year after ZimVie tapped Brainlab to add its surgical guidance technology to ZimVie’s own spinal surgery devices, the partnership has already paid off. The first product of their ...

The Food and Drug Administration cleared 37 orthopedic- and spine-related devices in September. 1. Clydesdale Spinal System from Medtronic. 2. Longbow Spacer System from Life Spine. 3. Genesys Spine ...

Life Spine, a medtech company focused on the surgical treatment of spinal disorders, recently announced the FDA clearance to market its ARx Sacral Alar Iliac (SAI) Spinal Fixation System. The system, ...

BORDEAUX, France & BOSTON--(BUSINESS WIRE)-- Regulatory News: IMPLANET (Euronext Growth: ALIMP, FR0013470168, eligible for PEA-PME equity savings plans), a medical technology company specializing in ...

ZimVie (NASDAQ:ZIMV) said it has received FDA clearance for its Vital Spinal Fixation System, including instruments for use with Brainlab’s Spine & Trauma Navigation product. The medical device maker ...

WEST CHESTER, PA — Centinel Spine®, LLC has received U.S. Food and Drug Administration (FDA) Premarket Approval for two-level indications of its prodiscC Vivo and prodiscC SK cervical total disc ...

Please provide your email address to receive an email when new articles are posted on . The draft guidance is for class II non-resorbable, non-spinal bone plate and screw systems, stand-alone bone ...

Please provide your email address to receive an email when new articles are posted on . The FDA has announced a final order to classify the screw sleeve bone fixation device into class II with special ...