30 Day Trial
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Monthly compilations are available in PDF form.

Reimbursement / Regulatory

NLT SPINE obtained FDA 510(k) clearance to market next-generation versions of its PROW FUSION™ and eSPIN™ devices for lumbar interbody fusion. Enhancements include new designs and materials, fewer instruments, additional irrigation capability and optimized cutting tip design. (NLT Spine Ltd., 10/30/13)