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.

Surgalign’s HOLO AI Insights is designed to enhance clinical decision making through artificial intelligence technology.

One hundred new plates for foot, ankle, hand and wrist indications are included in the company’s latest 510(k) clearance.

OC Spine announced the first clinical cases of their recently-cleared Focus Interbody system featuring the xCELLerate bioactive coating.

The Caduceus S AR Spine Navigation System utilizes 2D C-arm imaging technology to create a precise map of the patient’s spine.

The laser-etched cryopreserved osteochondral allograft showed positive patient-reported outcomes in prospective clinical study.