{"id":2917,"date":"2019-04-26T22:30:00","date_gmt":"2019-04-26T22:30:00","guid":{"rendered":"https:\/\/www.xvivogroup.com\/us\/mfn_news\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/"},"modified":"2019-04-26T22:30:00","modified_gmt":"2019-04-26T22:30:00","slug":"xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2","status":"publish","type":"mfn_news","link":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/","title":{"rendered":"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122"},"content":{"rendered":"
On April 26, 2019 XVIVO received Premarket approval (PMA) from the FDA for the products XPS\u2122 and STEEN Solution\u2122 for sale on the American market. The approval means that STEEN Solution\u2122, XPS\u2122 and the accompanying single-use articles are the only medical device products that are approved for Ex Vivo Lung Perfusion (EVLP) of initially unacceptable donated lungs at body temperature.<\/strong><\/div>\n

Please see FDA press release on the following link:\u00a0
https:\/\/www.fda.gov\/news-events\/press-announcements\/fda-approves-device-help-increase-access-more-lungs-transplant<\/a><\/span><\/p>\n

Just over 40 percent of all lung transplantations worldwide are carried out in the USA. The products have already received regulatory approvals on all major markets and was previously sold on the US market under an HDE (Humanitarian Device Exemption) that entailed certain restrictions. A PMA will no longer entail any such restrictions.<\/span><\/p>\n

After several years of product development in close collaboration with experienced transplantation centers, and subsequent comprehensive clinical studies in the USA to verify both product and patient safety, XPS\u2122 and STEEN Solution\u2122 have received FDA Premarket Approval. The work on obtaining market approval from the FDA was started in 2009 and an HDE approval was received in August 2014. During the process, clinical studies have been carried out to demonstrate product and patient safety, and in March 2014 the FDA\u2019s Advisory Panel voted unanimously that XPS\u2122 and STEEN Solution\u2122 meet the requirements for HDE approval. <\/span><\/p>\n

An HDE approval entails certain restrictions, amongst other things that no more than 8,000 patients may be treated per year under HDE approval and that separate institutional IRB approval may be required for treatment. A PMA will no longer entail any such restrictions. After yesterday\u2019s approval, the products may now be sold in the American market without those restrictions.<\/span><\/p>\n

EVLP with STEEN Solution\u2122 are used in several hundred lung transplantations over the world every year. The NOVEL Extension study which completed enrollment in June 2017 involves follow-up of the patients for up to one year. XVIVO Perfusion\u2019s will perform a PAS (Post Approval Study) as required by the FDA to follow up the long-term characteristics through an official register in the USA comparing traditionally preserved donated lungs with those where EVLP has been performed before transplantation. <\/span><\/p>\n

\u201cIt is a breakthrough for XVIVO that we have now received an PMA from the FDA and can sell STEEN Solution\u2122 and XPS\u2122 in the American market without any restrictions. The approval of the PMA application was the goal of a ten-year effort with the company\u2019s largest multicenter study ever performed in the largest market in the world, a huge effort from the organization and is therefore an very important milestone for the company\u201d says Dr. Magnus Nilsson, CEO of XVIVO Perfusion AB.<\/span><\/p>\n

April 27, 2019
<\/span>Gothenburg
XVIVO Perfusion AB (publ)
Magnus Nilsson, CEO<\/p>\n

\n

For further information please contact:<\/span><\/p>\n

Christoffer Rosenblad, CFO, +46 735 192159, christoffer.rosenblad@xvivoperfusion.com
Magnus Nilsson, CEO, +46 31 788 2150, magnus.nilsson@xvivoperfusion.com<\/span>
For further information on XVIVO Perfusion\u2019s business, please refer to the company\u2019s website, www.xvivoperfusion.com<\/span><\/p>\n

This information is information that Xvivo Perfusion AB (publ) is obliged to make public pursuant to the EU Market Abuse Regulation.\u00a0\u00a0The information was submitted for publication, through the agency of the contact person set out above, at 12:30 am CET on April 27, 2019.<\/span><\/p>\n

This is a translation of the Swedish version of the press release. When in doubt, the Swedish wording prevails.<\/span><\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

On April 26, 2019 XVIVO received Premarket approval (PMA) from the FDA for the products XPS\u2122 and STEEN Solution\u2122 for…<\/p>\n","protected":false},"template":"","class_list":["post-2917","mfn_news","type-mfn_news","status-publish","hentry","mfn-news-tag-mfn","mfn-news-tag-mfn-type-ir","mfn-news-tag-mfn-lang-en","mfn-news-tag-mfn-regulatory","mfn-news-tag-mfn-regulatory-mar","mfn-news-tag-mfn-ci","mfn-news-tag-mfn-ci-other"],"acf":[],"yoast_head":"\nXVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122 - XVIVO<\/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.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122 - XVIVO\" \/>\n<meta property=\"og:description\" content=\"On April 26, 2019 XVIVO received Premarket approval (PMA) from the FDA for the products XPS\u2122 and STEEN Solution\u2122 for...\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/\" \/>\n<meta property=\"og:site_name\" content=\"United States\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/pressreleases\\\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\\\/\",\"url\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/pressreleases\\\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\\\/\",\"name\":\"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122 - XVIVO\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/#website\"},\"datePublished\":\"2019-04-26T22:30:00+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/pressreleases\\\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/pressreleases\\\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/pressreleases\\\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/#website\",\"url\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/\",\"name\":\"United States\",\"description\":\"\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.xvivogroup.com\\\/us\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122 - XVIVO","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/","og_locale":"en_US","og_type":"article","og_title":"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122 - XVIVO","og_description":"On April 26, 2019 XVIVO received Premarket approval (PMA) from the FDA for the products XPS\u2122 and STEEN Solution\u2122 for...","og_url":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/","og_site_name":"United States","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"3 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/","url":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/","name":"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122 - XVIVO","isPartOf":{"@id":"https:\/\/www.xvivogroup.com\/us\/#website"},"datePublished":"2019-04-26T22:30:00+00:00","breadcrumb":{"@id":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.xvivogroup.com\/us\/pressreleases\/xvivo-has-received-market-approval-pma-from-the-fda-for-steen-solution-and-xps-2\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.xvivogroup.com\/us\/"},{"@type":"ListItem","position":2,"name":"XVIVO has received market approval (PMA) from the FDA for STEEN Solution\u2122 and XPS\u2122"}]},{"@type":"WebSite","@id":"https:\/\/www.xvivogroup.com\/us\/#website","url":"https:\/\/www.xvivogroup.com\/us\/","name":"United States","description":"","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.xvivogroup.com\/us\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"}]}},"_links":{"self":[{"href":"https:\/\/www.xvivogroup.com\/us\/wp-json\/wp\/v2\/mfn_news\/2917","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.xvivogroup.com\/us\/wp-json\/wp\/v2\/mfn_news"}],"about":[{"href":"https:\/\/www.xvivogroup.com\/us\/wp-json\/wp\/v2\/types\/mfn_news"}],"wp:attachment":[{"href":"https:\/\/www.xvivogroup.com\/us\/wp-json\/wp\/v2\/media?parent=2917"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}