{"id":571,"date":"2011-06-30T18:00:00","date_gmt":"2011-06-30T18:00:00","guid":{"rendered":"http:\/\/chicagotraumas.wpengine.com\/olympus-biotech-exhibitor\/"},"modified":"2013-05-13T13:00:35","modified_gmt":"2013-05-13T13:00:35","slug":"olympus-biotech-exhibitor","status":"publish","type":"post","link":"https:\/\/chicagotraumasymposium.com\/index.php\/olympus-biotech-exhibitor\/","title":{"rendered":"Olympus Biotech- Exhibitor"},"content":{"rendered":"<div><span>Olympus Biotech Corporation is dedicated to the further advancement of orthopedics and regenerative medicine to improve the lives\u00a0<\/span><span>of patients around the world.\u00a0 Olympus Biotech markets and sells OP-1\u2122 Putty and OP-1\u2122 Implant which are currently approved in the\u00a0<\/span><country-region w:st=\"on\"><place w:st=\"on\"><span>U.S.<\/span><\/place><\/country-region><span>\u00a0under Humanitarian Device Exemptions (HDEs) for revision posterolateral lumbar spine fusion and for the treatment of long bone<\/span><\/div>\n<div><span>nonunions, respectively.\u00a0 OP-1 is also approved in\u00a0<\/span><country-region w:st=\"on\"><span>Australia<\/span><\/country-region><span>\u00a0and\u00a0<\/span><country-region w:st=\"on\"><span>Canada<\/span><\/country-region><span>\u00a0as OP-1 Implant, and in\u00a0<\/span><country-region w:st=\"on\"><place w:st=\"on\"><span>Switzerland<\/span><\/place><\/country-region><span>\u00a0and the European Union\u00a0<\/span><span>as Osigraft and Opgenra.\u00a0 Approximately 40,000 patients have been treated globally with OP-1 Products.<\/span><\/div>\n<div><span><br \/><\/span><\/div>\n<div><span>Learn more at\u00a0<\/span><a href=\"http:\/\/www.op1.com\/\"><span><span>http:\/\/www.op1.com\/<\/span><\/span><\/a><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Olympus Biotech Corporation is dedicated to the further advancement of orthopedics and regenerative medicine to improve the lives\u00a0of patients around the world.\u00a0 Olympus Biotech markets and sells OP-1\u2122 Putty and OP-1\u2122 Implant which are currently approved in the\u00a0U.S.\u00a0under Humanitarian Device Exemptions (HDEs) for revision posterolateral lumbar spine fusion and for the treatment of long bone [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3,1],"tags":[],"class_list":["post-571","post","type-post","status-publish","format-standard","hentry","category-blog","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v16.6.1 - 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