Title: 10ο Παγκοσμιο Συνεδριο Αποστειρωσης
Location: Ξενοδοχειο Creta & Terra Maris – Κρητη
Start Date: 2009-10-07
End Date: 2009-10-10
10ο Παγκοσμιο Συνεδριο Αποστειρωσης
– September 2, 2009Posted in: agenda
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Product Launch
- Ortho Kinematics Receives FDA 510(k) Clearance for KineGraph VMA System
January 20, 2012 | 09:37
Tweet Share AUSTIN, Texas–(Healthcare Sales & Marketing Network)– Ortho Kinematics‚ a private company focused on... - Medtronic Announces Global Launch of the T2 ALTITUDE Expandable Corpectomy Device
November 15, 2011 | 10:07
Tweet Share The latest advancement in expandable cage technology for surgeons, hospitals and patients ... - Medtronic Introduces New Procedure for Minimally Invasive Spinal Fusion
November 3, 2011 | 10:08Tweet Share MEMPHIS, Tenn.–(Healthcare Sales & Marketing Network)– Medtronic, Inc. (NYSE:MDT ) the world leader...
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Archive for Product Launch »
- Ortho Kinematics Receives FDA 510(k) Clearance for KineGraph VMA System
Publications
- For Back, Neck Pain, Artificial Disc Replacement Has Cost, Outcome Advantages Over Fusion Surgery
- Surgical assessment of the proximal thoracic curve in adolescent idiopathic scoliosis
- Percutaneous core excision and radiofrequency thermo-coagulation for the ablation of osteoid osteoma of the spine
- Erythropoietin in spinal cord injury
- Spinal synovial cysts: pathogenesis, diagnosis and surgical treatment in a series of seven cases and literature review
- Scheuermann’s disease: focus on weight and height role
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FDA
- FDA Grants Eden Spine 510(K) Clearance for Its New Vertebral Body Replacement
February 6, 2012 | 11:25Tweet Share Eden Spine launches in the United States its proprietary Vertebral Body Replacement (VBR),…
- Interventional Spine®, Inc. Announces Issuance of Patent Covering the Company’s Expandable Interbody Fusion Device, the Opticage(TM)
February 6, 2012 | 11:04Tweet Share IRVINE, Calif., Jan. 31, 2012 /PRNewswire via COMTEX/ — Interventional Spine®, Inc. today…
- Medtronic Announces 510(k) Clearance for the Aquamantys SBS 5.0 Sheathed Bipolar Sealer for Spine Surgery
January 30, 2012 | 15:02Tweet Share MINNEAPOLIS–(Healthcare Sales & Marketing Network)– Medtronic, Inc. (NYSE:MDT ) announced today that it…
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Archive for FDA »
- FDA Grants Eden Spine 510(K) Clearance for Its New Vertebral Body Replacement
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