FDAnews Device Daily Bulletin
Medical Devices / Submissions and Approvals

FDA Clears Implanet’s Screw Securing Device for Vertebral Fusion 

March 21, 2019
A A

The FDA granted Implanet 510(k) clearance for another product in the company’s Jazz product range, the Jazz Cap system, a device used for securing screws in poor-quality bone.

The product consists of a set of single-use sterile implants that support the treatment of degenerative conditions in patients.

The implants are composed of a band, a screw, and the company’s patented locking mechanism.

View today's stories