


NLT SPINE Receives 510(k) Clearance for Its Lumbar Interbody Fusion Device ... MarketWatch (press release) KFAR SABA, Israel, Feb 01, 2012 (BUSINESS WIRE) -- NLT SPINE, a developer of Minimally Invasive Spine Surgery (MISS) products, today announced that its PROW FUSION(TM) device received 510(k) clearance from the US Food and Drug Administration (FDA). |
NLT SPINE Receives 510(k) Clearance for Its Lumbar Interbody Fusion Device ... EON: Enhanced Online News (press release) KFAR SABA, Israel--(EON: Enhanced Online News)--NLT SPINE, a developer of Minimally Invasive Spine Surgery (MISS) products, today announced that its PROW FUSION™ device received 510(k) clearance from the US Food and Drug Administration (FDA). NLT Spine Receives FDA Clearance for Minimally Invasive TLIF System |
World Cancer Day 2012: Imaging technique which can diagnose brain cancer ... India.Com Health A new technique diagnoses brain tumours non-invasively, eliminating the need for surgery in patients whose tumours are located in areas too dangerous for biopsy. The new magnetic resonance spectroscopy (MRS) technique provides a definitive diagnosis of ... |