{"id":470557,"date":"2021-04-05T07:03:25","date_gmt":"2021-04-05T11:03:25","guid":{"rendered":"http:\/\/www.marketnewsdesk.com\/?p=470557"},"modified":"2021-04-05T07:03:25","modified_gmt":"2021-04-05T11:03:25","slug":"orthofix-announces-fda-clearance-and-initial-patient-implant-of-the-companys-first-3d-printed-titanium-cervical-spacer-system-with-nanovate-technology","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/orthofix-announces-fda-clearance-and-initial-patient-implant-of-the-companys-first-3d-printed-titanium-cervical-spacer-system-with-nanovate-technology\/","title":{"rendered":"Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology"},"content":{"rendered":"<p>        <!--.bwalignc { text-align: center; list-style-position: inside }\n.bwlistdisc { list-style-type: disc }body {font:normal small Arial,Helvetica,sans-serif;color:#000;background-color:#fff;padding:24px;margin:0;} a img {border:0;} h3 {font-size:medium;color:#000;margin:0 0 1em 0; text-align:center;}-->  <\/p>\n<p class=\"bwalignc\"><b>Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology<\/b><\/p>\n<p><i>Designed with nanoscale surface features, the CONSTRUX Mini Ti System is Orthofix\u2019s first 3D-printed titanium (Ti) interbody introduced to the market.<\/i><\/p>\n<p>LEWISVILLE, Texas&#8211;(<a href=\"http:\/\/www.businesswire.com\">BUSINESS WIRE<\/a>)&#8211;<a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Forthofix.com%2F&amp;esheet=52405670&amp;newsitemid=20210405005029&amp;lan=en-US&amp;anchor=Orthofix+Medical+Inc&amp;index=1&amp;md5=36103e52e302a92f2c8e6dc092bc5539\">Orthofix Medical Inc<\/a>. (NASDAQ:OFIX), a global medical device company with a spine and extremities focus, today announced the U.S. Food and Drug Administration (FDA) 510(k) clearance and the first patient implant of the 3D-printed <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.orthofix.com%2Fifus%2Fconstrux-mini-ti-spacer-system%2F&amp;esheet=52405670&amp;newsitemid=20210405005029&amp;lan=en-US&amp;anchor=CONSTRUX%26%238482%3B+Mini+Ti+Spacer+System&amp;index=2&amp;md5=3ad27bbf6baf2033d8ecd6ff1a86ac56\">CONSTRUX<sup>\u2122<\/sup> Mini Ti Spacer System<\/a>. Developed to enhance anterior cervical discectomy and fusion (ACDF) procedures, the CONSTRUX Mini Ti cervical spacer with Nanovate<sup>\u2122<\/sup> Technology is the first 3D-printed titanium interbody introduced to the market by Orthofix.\n<\/p>\n<p id=\"news-body-cta\">This press release features multimedia. View the full release here: <a href=\"https:\/\/www.businesswire.com\/news\/home\/20210405005029\/en\/\" rel=\"nofollow\">https:\/\/www.businesswire.com\/news\/home\/20210405005029\/en\/<\/a><\/p>\n<div id=\"bwbodyimg\" style=\"width: 480px;float:left;padding-left:0px;padding-right:20px;padding-top:0px;padding-bottom:0px\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20210405005029\/en\/868924\/4\/CONSTRUX_Mini_Ti.jpg\" alt=\"Image of Orthofix\u2019s first 3D-printed titanium interbody, the CONSTRUX\u2122 Mini Ti Cervical Spacer System with Nanovate\u2122 Technology. (Photo: Orthofix Medical Inc.)\" \/><\/p>\n<p style=\"font-size:85%\">Image of Orthofix\u2019s first 3D-printed titanium interbody, the CONSTRUX\u2122 Mini Ti Cervical Spacer System with Nanovate\u2122 Technology. (Photo: Orthofix Medical Inc.)<\/p>\n<\/div>\n<p>\n\u201cThe ACDF procedure, which is often used to treat a herniated cervical disc or degenerative disc disease, involves replacing a patient\u2019s damaged cervical disc with an interbody packed with a biologic to promote fusion in order to provide stability and strength to the area,\u201d said Wayne Cheng, M.D., an orthopedic spine surgeon operating at Loma Linda University Medical Center in Loma Linda, CA, who performed the first patient implant procedure. \u201cThe CONSTRUX Mini Ti System\u2019s optimized porosity and surface allows bone to grow into and through the spacer in order to aid with the patient\u2019s fusion.\u201d\n<\/p>\n<p>\nThe CONSTRUX Mini Ti Spacer System with Nanovate Technology is one of many Orthofix products with nanotechnology FDA clearance including the CONSTRUX<sup>\u2122<\/sup> Mini PTC Spacer System, the Pillar<sup>\u2122<\/sup> SA PTC Spacer System, and the FORZA<sup>\u2122<\/sup> PTC Spacer System. When compared to solid PEEK devices, the 3D-printed endplates of these implants with Nanovate Technology show a significant increase in growth factors involved in osteogenesis and osteoblast maturation resulting in a more favorable osteogenic environment for bone ingrowth.\n<\/p>\n<p>\n\u201cOrthofix\u2019s cervical spine offerings feature a wide array of implants ranging from motion-preserving products like the M6-C<sup>\u2122<\/sup> artificial cervical disc to advanced interbody and fixation solutions that aid surgeons in restoring spinal alignment and decreasing pain and nerve compression,\u201d said Orthofix President of Global Spine Kevin Kenny. \u201cWe are dedicated to expanding our comprehensive cervical spine solutions with technologies like the CONSTRUX Mini Ti Spacer System that can make a meaningful difference in our product offerings and in the lives of patients.\u201d\n<\/p>\n<p>\nThe CONSTRUX Mini Ti Spacer System features include:\n<\/p>\n<ul class=\"bwlistdisc\">\n<li>\n3D-printed porous titanium with macro, micro, and nanoscale surface features\n<\/li>\n<li>\nNanoscale surface that has been shown to increase proliferation and alkaline phosphatase activity (an early osteogenic differentiation marker) in human stem cells in vitro*\n<\/li>\n<li>\nEndplates with 400 micron pores and 50-percent porosity designed to help facilitate bone ingrowth**\n<\/li>\n<li>\nFunctional gradient porous structure with 80-percent porosity at the midline of the implant which allows for increased fluoroscopic visualization\n<\/li>\n<li>\nLarge center opening with concaved inner walls for packing bone-grafting material\n<\/li>\n<li>\nStraightforward instrumentation for easy implantation\n<\/li>\n<\/ul>\n<p>\nOrthofix offers a comprehensive cervical portfolio with differentiated technologies across biologics, bone growth therapies and spinal implants. Learn more about our cervical solutions by visiting <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.orthofix.com%2F&amp;esheet=52405670&amp;newsitemid=20210405005029&amp;lan=en-US&amp;anchor=Orthofix.com&amp;index=3&amp;md5=569ee3b765bc74de44d300b60fa38566\">Orthofix.com<\/a>.\n<\/p>\n<p>\n*As suggested in an in vivo ovine lumbar spinal fusion model\n<\/p>\n<p>\n**In vitro performance may not be representative of clinical performance\n<\/p>\n<p><b>About Orthofix<\/b><\/p>\n<p>\nOrthofix Medical Inc. is a global medical device and biologics company with a spine and extremities focus. The Company\u2019s mission is to deliver innovative, quality-driven solutions as we partner with health care professionals to improve patients\u2019 lives. Headquartered in Lewisville, Texas, Orthofix\u2019s spine and orthopedic extremities products are distributed in more than 70 countries via the Company\u2019s sales representatives and distributors. For more information, please visit <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Fwww.Orthofix.com&amp;esheet=52405670&amp;newsitemid=20210405005029&amp;lan=en-US&amp;anchor=www.Orthofix.com&amp;index=4&amp;md5=bc21123c27dacf4aa59eafc05874636e\">www.Orthofix.com<\/a>.\n<\/p>\n<p><b>Forward-Looking Statements<\/b><\/p>\n<p>\nThis communication contains forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended, relating to our business and financial outlook, which are based on our current beliefs, assumptions, expectations, estimates, forecasts and projections. In some cases, you can identify forward-looking statements by terminology such as \u201cmay,\u201d \u201cwill,\u201d \u201cshould,\u201d \u201cexpects,\u201d \u201cplans,\u201d \u201canticipates,\u201d \u201cbelieves,\u201d \u201cestimates,\u201d \u201cprojects,\u201d \u201cintends,\u201d \u201cpredicts,\u201d \u201cpotential,\u201d or \u201ccontinue\u201d or other comparable terminology. These forward-looking statements are not guarantees of our future performance and involve risks, uncertainties, estimates and assumptions that are difficult to predict, including the risks described in Part I, Item 1A under the heading Risk Factors in our Annual Report on Form 10-K for the year ended December 31, 2020 (the \u201c2020 Form 10-K\u201d). In addition to the risks described there, factors that could cause or contribute to such differences may include, but are not limited to: the risk that surgeons may be slow to adopt the CONSTRUX Mini Ti Spacer System; the risk that future patient studies or clinical experience and data may indicate that treatment with the CONSTRUX Mini Ti Spacer System does not improve patient outcomes as much as previously believed, or otherwise call into question the benefits of its use to patients, hospitals and surgeons; the risk that the product may not perform as intended and may therefore not achieve commercial success; the risk that competitors may develop superior products or may have a greater market position enabling more successful commercialization; the risk that insurance payers may decline to reimburse healthcare providers for the use of our products.\n<\/p>\n<p>\nThis list of risks, uncertainties and other factors is not complete. We discuss some of these matters more fully, as well as certain risk factors that could affect our business, financial condition, results of operations, and prospects, in reports we file from time-to-time with the SEC, which are available to read at <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Fwww.sec.gov&amp;esheet=52405670&amp;newsitemid=20210405005029&amp;lan=en-US&amp;anchor=www.sec.gov&amp;index=5&amp;md5=319c92627a993e0564bce044e06891de\">www.sec.gov<\/a>. Any or all forward-looking statements that we make may turn out to be wrong (due to inaccurate assumptions that we make or otherwise), and our actual outcomes and results may differ materially from those expressed in these forward-looking statements. You should not place undue reliance on any of these forward-looking statements. Further, any forward-looking statement speaks only as of the date hereof, unless it is specifically otherwise stated to be made as of a different date. We undertake no obligation to update, and expressly disclaim any duty to update, our forward-looking statements, whether as a result of circumstances or events that arise after the date hereof, new information, or otherwise.\n<\/p>\n<p><img decoding=\"async\" alt=\"\" src=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20210405005029r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\" style=\"width:0;height:0\" \/><span class=\"bwct31415\" \/><\/p>\n<p id=\"mmgallerylink\"><span id=\"mmgallerylink-phrase\">View source version on businesswire.com: <\/span><span id=\"mmgallerylink-link\"><a href=\"https:\/\/www.businesswire.com\/news\/home\/20210405005029\/en\/\" rel=\"nofollow\">https:\/\/www.businesswire.com\/news\/home\/20210405005029\/en\/<\/a><\/span><\/p>\n<p>\nAlexa Huerta<br \/>\n<br \/>Investor Relations<br \/>\n<br \/>Tel 214 937 3190<br \/>\n<br \/><a rel=\"nofollow\" href=\"mailto:alexahuerta@orthofix.com\">alexahuerta@orthofix.com<br \/>\n<\/a><\/p>\n<p>\nDenise Landry<br \/>\n<br \/>Media Relations<br \/>\n<br \/>Tel 214 937 2529<br \/>\n<br \/><a rel=\"nofollow\" href=\"mailto:deniselandry@orthofix.com\">deniselandry@orthofix.com<\/a><\/p>\n<p><b>KEYWORDS:<\/b> United States North America Texas<\/p>\n<p><b>INDUSTRY KEYWORDS:<\/b> FDA Health Medical Devices<\/p>\n<p><b>MEDIA:<\/b><\/p>\n<table cellpadding=\"3\" cellspacing=\"3\">\n<tr>\n<td><font face=\"Arial\" size=\"2\"><b>Logo<\/b><\/font><\/td>\n<\/tr>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20210405005029\/en\/760684\/3\/Orthofix_Line_Logo.jpg\" alt=\"Logo\" \/><\/td>\n<\/tr>\n<tr>\n<td><font face=\"Arial\" size=\"2\"><\/font><\/td>\n<\/tr>\n<tr>\n<td><font face=\"Arial\" size=\"2\"><b>Photo<\/b><\/font><\/td>\n<\/tr>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20210405005029\/en\/868924\/3\/CONSTRUX_Mini_Ti.jpg\" alt=\"Photo\" \/><\/td>\n<\/tr>\n<tr>\n<td><font face=\"Arial\" size=\"2\">Image of Orthofix\u2019s first 3D-printed titanium interbody, the CONSTRUX\u2122 Mini Ti Cervical Spacer System with Nanovate\u2122 Technology. (Photo: Orthofix Medical Inc.)<\/font><\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"<p>Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology Designed with nanoscale surface features, the CONSTRUX Mini Ti System is Orthofix\u2019s first 3D-printed titanium (Ti) interbody introduced to the market. LEWISVILLE, Texas&#8211;(BUSINESS WIRE)&#8211;Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and extremities focus, today announced the U.S. Food and Drug Administration (FDA) 510(k) clearance and the first patient implant of the 3D-printed CONSTRUX\u2122 Mini Ti Spacer System. Developed to enhance anterior cervical discectomy and fusion (ACDF) procedures, the CONSTRUX Mini Ti cervical spacer with Nanovate\u2122 Technology is the first 3D-printed titanium interbody introduced to the market by Orthofix. This press release features multimedia. View the &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/orthofix-announces-fda-clearance-and-initial-patient-implant-of-the-companys-first-3d-printed-titanium-cervical-spacer-system-with-nanovate-technology\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-470557","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/orthofix-announces-fda-clearance-and-initial-patient-implant-of-the-companys-first-3d-printed-titanium-cervical-spacer-system-with-nanovate-technology\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Orthofix Announces FDA Clearance and Initial Patient Implant of the Company\u2019s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology Designed with nanoscale surface features, the CONSTRUX Mini Ti System is Orthofix\u2019s first 3D-printed titanium (Ti) interbody introduced to the market. LEWISVILLE, Texas&#8211;(BUSINESS WIRE)&#8211;Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and extremities focus, today announced the U.S. Food and Drug Administration (FDA) 510(k) clearance and the first patient implant of the 3D-printed CONSTRUX\u2122 Mini Ti Spacer System. Developed to enhance anterior cervical discectomy and fusion (ACDF) procedures, the CONSTRUX Mini Ti cervical spacer with Nanovate\u2122 Technology is the first 3D-printed titanium interbody introduced to the market by Orthofix. This press release features multimedia. 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LEWISVILLE, Texas&#8211;(BUSINESS WIRE)&#8211;Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and extremities focus, today announced the U.S. Food and Drug Administration (FDA) 510(k) clearance and the first patient implant of the 3D-printed CONSTRUX\u2122 Mini Ti Spacer System. Developed to enhance anterior cervical discectomy and fusion (ACDF) procedures, the CONSTRUX Mini Ti cervical spacer with Nanovate\u2122 Technology is the first 3D-printed titanium interbody introduced to the market by Orthofix. This press release features multimedia. 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