Crosstrees Medical Receives FDA 510(k) Clearance for Pod System

Boulder, Colo.-based Crosstrees Medical received FDA 510(k) clearance for its Percutaneous Vertebral Augmentation Pod System.

Advertisement

Clearance came after an investigational device exemption study of 135 patients in four countries, including the U.S.

The Pod aims to be an improved vertebral fracture repair device.

More Articles on Supply Chain:
K2M Spinal Deformity Device Implanted in First French Hospital Procedure
Vivex Biomedical Raises $7.4M for Stem Cell, Implant Technologies
Alphatec Holdings to Reduce Workforce, Operating Expenses for French Affiliate

Advertisement

Next Up in Uncategorized

Advertisement

Comments are closed.