Spinal Tech

The FDA recently granted NuVasive 510(k) clearance to expand its CoRent Small Interlock system for multilevel use in cervical spine surgery.

A federal appeals court on Nov. 20 reinstated a woman's design-defect lawsuit over a Zimmer Biomet hip prosthesis implanted in her in 2011, reports Mass Device.

The FDA provided Think Surgical 510(k) clearance to market its TSolution One total knee application for total knee arthroplasty in the U.S.

Exactech acquired its independent distribution partner in Italy to create a new corporate subsidiary. 

Although Aurora Spine posted $2.5 million in third-quarter 2019 revenues, the company still realized a $417,399 loss.

The FDA awarded Think Surgical FDA 510(k) clearance for its TSolution One Total Knee Application, which incorporates 3D presurgical planning software into a knee replacement procedure.

The FDA expanded its clearance for NuVasive's CoRoent Small Interlock system to allow for on-label use of the device at multiple contiguous spinal levels.

Here are three orthopedic and spine device companies that recently launched or released devices:

Fuse Medical recently ranked 89th in Deloitte's 2019 Technology Fast 500 list of fastest growing companies in North America, reports the Valdosta Daily Times.

The world's biggest medical device companies made more than $542.6 million in general payments to physicians and hospitals in 2018, according to MassDevice's analysis of the Medical Design & Outsourcing Big 100 list and CMS Open Payments data.