Tyber Medical has achieved a significant milestone with the MDR CE Mark certification from BSI for its PEEK Titanium Plasma-coated cervical cages. This Class III device is designed for cervical spine levels C2 to T1. It combines a PEEK core with an advanced Titanium Plasma coating to enhance bone cell response and facilitate effective spinal fusion. This certification aligns Tyber Medical\u2019s products with stringent EU regulatory standards for quality and performance, bolstering its position in the global market.<\/p>\n\n\n\n
The MDR clearance is backed by extensive clinical evidence, including data from over 150 patients in Tyber Medical’s clinical registry, demonstrating an impressive fusion rate of over 98%. This achievement validates the safety and efficacy of the PEEK Titanium Plasma-coated cervical cages, reinforcing Tyber Medical\u2019s dedication to advancing spinal care through innovative, data-driven solutions. The device exemplifies the company’s commitment to enhancing patient outcomes with reliable and accessible medical technologies.<\/p>\n\n\n\n
“Receiving MDR certification for our PEEK Titanium Plasma-coated cervical cages marks a pivotal achievement for our organization,” said Jeff Tyber, CEO and President of Tyber Medical. “This accomplishment enables us to bring our cutting-edge solutions to healthcare providers and patients worldwide, demonstrating our unwavering commitment to innovation and excellence in medical device technology.”<\/p>\n","protected":false},"excerpt":{"rendered":"
Tyber Medical secures MDR CE Mark certification for PEEK Titanium Plasma-coated cervical cages, advancing spinal fusion technology and expanding access to global markets.<\/p>\n","protected":false},"author":2,"featured_media":16201,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"colormag_page_layout":"default_layout","footnotes":""},"categories":[6,711],"tags":[704],"class_list":["post-32090","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-europe","category-orthopaedics","tag-ce-mark"],"_links":{"self":[{"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/posts\/32090","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/comments?post=32090"}],"version-history":[{"count":4,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/posts\/32090\/revisions"}],"predecessor-version":[{"id":40211,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/posts\/32090\/revisions\/40211"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/media\/16201"}],"wp:attachment":[{"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/media?parent=32090"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/categories?post=32090"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/g-medtech.com\/news\/wp-json\/wp\/v2\/tags?post=32090"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}