Further, the USPTO intends to grant a patent for the conversion of the design from a hemi-arthroplasty to a total arthroplasty.

The system enables flexible treatment of fractures of the distal humerus and olecranon important to the elbow function and stability.

A new clinical study demonstrates Medacta’s MySpine accuracy in screw replacement during spine revision surgery.

The expanded clearance extends the clinical benefits of Precice to a wider range of patients, namely pediatrics.

The next iteration of HOLO Portal delivers advancements based on early clinical experience and insights from leading spine surgeons in the U.S.

FDA has issued a 510(k) clearance to Accelus for its Remi Robotic Navigation System for use with GE OEC 9900 C-Arm fluoroscopic imaging systems.

With multiple sizes and configurations, the vallos allograft line allows clinicians to choose exactly what they need for each procedure.

Ogmend is an implantable sleeve to aid screw fixation in challenging scenarios. The device will be made available in the U.S. through a staged release.

The Tether device is now deemed “medically necessary” for the treatment of pediatric scoliosis in additional patients covered by Highmark and BCBS North Dakota.

OssDsign has reached 200 implants of its 3D-printed titanium patient-specific cranial implant in France.