30 Day Trial
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Monthly compilations are available in PDF form.

Reimbursement / Regulatory

Centinel Spine received FDA 510(k) clearance for its STALIF MIDLINE®, MIDLINE II™ and MIDLINE II-Ti™ (Ti-ACTIVE™) devices for use with allogeneic bone graft in lumbar spinal fusion. (Centinel Spine, Inc., 6/17/15)