Zimmer Biomet issued a voluntary field safety corrective action for certain ROSA Brain, Spine and One surgical robotic devices due to internal identification of an issue that may prevent the robot arm from reaching a desired position. The issue has not been identified in the field.
NuVasive is increasing investment in support of adult/pediatric spinal deformity research and education, and expects to launch the RELINE® Small Stature posterior fixation system this summer.
Phase III study results demonstrated that Anika Therapeutics’ CINGAL® provided superior immediate and short term OA pain relief after injection vs. hyaluronic acid alone, and superior relief at 26 weeks vs. saline.Â
Interim study results indicate that patients receiving Rotation Medical’s Bioinductive Implant to treat rotator cuff disease reported statistically significant improvement at six months.