Implanet Receives Expanded 510(k) Clearance for Jazz Spinal Implant

Implanet has received expanded 510(k) clearance from the FDA for its Jazz spinal implant, allowing it to be used with other pedicle screw and rod systems for thoraco-lumbar posterior fixation.

The implant was previously indicated solely for use with the Implanet Spine System.

The device provides temporary stabilization as a bone anchor during the development of solid bony fusion and aids in the repair of bone fractures.

Headquartered near Bordeaux, France, Implanet manufactures implants for orthopedic surgery. — Michael Cipriano