NeuroPro Spinal Jaxx Receives FDA Clearance for Spinal Fusion Device
NeuroPro Spinal Jaxx received FDA 510(k) clearance to market the Spinal Jaxx expandable intervertebral spacer.
Spinal Jaxx features instruments to load additional bone graft after implantation and expansion, a locking mechanism to prevent device collapse, titanium endplates and a claim of greater expansion capability than most competing products.
This represents NeuroPro's first 510(k) clearance. The company was among our 2011 ORTHOKNOW® line-up of New and Notables at the annual NASS meeting
Sources: NeuroPro Spinal Jaxx, Inc.; ORTHOWORLD Inc.