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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.

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