30 Day Trial

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Reimbursement / Regulatory

Precision Spine received FDA 510(k) clearance and commenced launch of the VAULT®-C Anterior Cervical Interbody Fusion Device. The integrated plate/cage design supports rigid screw fixation using a zero profile construct, which is intended to limit damage to surrounding vessels and adjacent soft tissue, while the large, open bone graft area allows for optimal graft containment. (Precision Spine, Inc., 10/15/14)