30 Day Trial

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Monthly compilations are available in PDF form.

Reimbursement / Regulatory

Centinel Spine received FDA 510(k) clearance for use of STALIF C® and STALIF C-TI™ interbody devices in multi-level cervical spinal fusion. The clearance represents the 1st cervical multilevel indication for a standalone interbody device by FDA. STALIF C was previously cleared for use with autograft or allogeneic bone graft at 1 level in patients with cervical degenerative disc disease. (Centinel Spine, Inc., 6/30/15)