Centinel Spine expanded its MIDLINE II-Ti product family, a Ti-ACTIVE™ coated, No-Profile, anterior lumbar Integrated Interbody device, in the U.S. and Australia.
Vertebral Technologies launched the InterLink™ pedicle screw system, including 22 polyaxial pedicle screws, 19 spinal rods, cross-connectors and set screws, to be used for single or multiple level fixation.
Integra LifeSciences launched the Integra® Fin-Lockâ„¢ Glenoid for the Titanâ„¢ Modular Shoulder System to address glenoid component loosening and failure in total shoulder arthroplasty.Â
Interventional Spine announced FDA clearance of the 80 Lumbar Lordotic Opticageâ„¢, an intervertebral body fusion device for use with autogenous bone graft in patients with degenerative disc disease.Â
Active Implants announced the first meniscus replacement in the SUN (Safety Using NUsurface®) clinical trial for patients with persistent knee pain following medial meniscus surgery.
Implanet received FDA 510(k) clearance and CE Mark approval for the Jazz Claw®, a hybrid implant designed to treat degenerative spinal pathologies.
Johnson & Johnson/JNJ's business review day on May 18 filled some gaps in my understanding of the restructuring picture, but some holes remain. Here is what we learned, and what we don't know yet.
Results from a 421-patient study revealed a 97.75% survival rate at 5 years for Medacta’s AMIStem hip implant. AMIStem has been implanted >100,000 times, to date.