10/9/2013 9:25:46 AM
PLAINSBORO, N.J., Oct. 9, 2013 (GLOBE NEWSWIRE) -- Integra LifeSciences Holdings Corporation (Nasdaq:IART) today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Integra® HollywoodTM NanoMetaleneTM Interbody Device (IBD), and expects to begin a controlled market release in the U.S. later this year. The IBD is used primarily in transforaminal lumbar interbody fusion (TLIF), a surgical procedure designed to help alleviate pain and nerve compression by fusing and stabilizing adjacent vertebrae in the lower back. Integra's newest IBD will be featured at the North American Spine Society (NASS) 28th annual meeting, October 9 – 12, 2013, in New Orleans, Louisiana.
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