{"id":496138,"date":"2021-05-20T06:03:06","date_gmt":"2021-05-20T10:03:06","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/"},"modified":"2021-05-20T06:03:06","modified_gmt":"2021-05-20T10:03:06","slug":"axonics-receives-fda-approval-further-expanding-mri-labeling","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/","title":{"rendered":"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling"},"content":{"rendered":"

<\/p>\n

Axonics\u00ae<\/sup> Receives FDA Approval Further Expanding MRI Labeling<\/b><\/p>\n

IRVINE, Calif.–(BUSINESS WIRE<\/a>)–
\nAxonics, Inc. (Nasdaq: AXNX), a global medical technology company that is developing and commercializing novel products for the treatment of bladder and bowel dysfunction, has received FDA approval allowing the use of detachable extremity coils for patients undergoing 1.5T and 3.0T MRI scans.\n<\/p>\n

\nThe FDA previously approved 1.5T and 3.0T MRI conditional labeling for using head and full-body transmit coils for the implantable components of the Axonics r-SNM\u00ae<\/sup> system.\n<\/p>\n

\nExtremity scans account for approximately 24% of all MRI scans performed today1<\/sup>. The expanded labeling now includes extremity scans using \u201cDetachable Upper and Lower Extremity Transmit\/Receive Coils.\u201d The expanded labeling is applicable to all previously implanted Axonics devices.\n<\/p>\n

\n\u201cThese additional conditions provide Axonics with the widest range of FDA approved MRI conditions in sacral neuromodulation,\u201d said Guangqiang Jiang, Ph.D., chief technology officer of Axonics. \u201cThe benefits of this labeling expansion include better image quality for extremity scans and increased scanning setup flexibility; broader MRI access for patients; and the avoidance of RF exposure of the entire body, which is important to patients who are frail, elderly, diabetic, obese, or pregnant as they are less tolerant to thermal stress from RF exposure. This approval further demonstrates Axonics\u2019 commitment to continuous innovation for the benefit of patients and clinicians.\u201d\n<\/p>\n

About Axonics<\/b><\/p>\n

\nBased in Irvine, Calif., Axonics is a global medical technology company that is developing and commercializing novel products for patients with bladder and bowel dysfunction. The company\u2019s rechargeable sacral neuromodulation (SNM) system provides patients suffering from overactive bladder and\/or fecal incontinence with long-lived, easy to use, safe, clinically effective therapy. In addition, Axonics\u2019 best-in-class urethral bulking agent, Bulkamid\u00ae<\/sup>, provides women suffering from stress urinary incontinence (SUI) with safe and durable symptom relief. Overactive bladder affects an estimated 87 million adults in the U.S. and Europe, with an additional 40 million adults estimated to suffer from fecal incontinence. SUI affects an estimated 20 million women in the U.S. alone. Axonics\u2019 clinically proven products are offered at hundreds of medical centers across the U.S. and abroad. Reimbursement coverage is well established in the U.S. and is a covered service in most European countries. For more information, visit www.axonics.com<\/a>.\n<\/p>\n

1<\/sup> IMV Benchmark Report MR 2018.\n<\/p>\n

\"\"<\/p>\n

View source version on businesswire.com: <\/span>https:\/\/www.businesswire.com\/news\/home\/20210520005152\/en\/<\/a><\/span><\/p>\n

Axonics contact<\/b>:
\n
Neil Bhalodkar
\n
949-336-5293
\n
ir@axonics.com<\/a><\/p>\n

KEYWORDS:<\/b> California United States North America<\/p>\n

INDUSTRY KEYWORDS:<\/b> Biotechnology FDA Health Medical Devices<\/p>\n

MEDIA:<\/b><\/p>\n\n\n\n\n
Logo<\/b><\/font><\/td>\n<\/tr>\n
\"Logo\"<\/td>\n<\/tr>\n
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Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling IRVINE, Calif.–(BUSINESS WIRE)– Axonics, Inc. (Nasdaq: AXNX), a global medical technology company that is developing and commercializing novel products for the treatment of bladder and bowel dysfunction, has received FDA approval allowing the use of detachable extremity coils for patients undergoing 1.5T and 3.0T MRI scans. The FDA previously approved 1.5T and 3.0T MRI conditional labeling for using head and full-body transmit coils for the implantable components of the Axonics r-SNM\u00ae system. Extremity scans account for approximately 24% of all MRI scans performed today1. The expanded labeling now includes extremity scans using \u201cDetachable Upper and Lower Extremity Transmit\/Receive Coils.\u201d The expanded labeling is applicable to all previously implanted Axonics devices. \u201cThese additional … <\/p>\n

Continue reading “Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling”<\/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-496138","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nAxonics\u00ae Receives FDA Approval Further Expanding MRI Labeling - 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\/axonics-receives-fda-approval-further-expanding-mri-labeling\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling IRVINE, Calif.–(BUSINESS WIRE)– Axonics, Inc. (Nasdaq: AXNX), a global medical technology company that is developing and commercializing novel products for the treatment of bladder and bowel dysfunction, has received FDA approval allowing the use of detachable extremity coils for patients undergoing 1.5T and 3.0T MRI scans. The FDA previously approved 1.5T and 3.0T MRI conditional labeling for using head and full-body transmit coils for the implantable components of the Axonics r-SNM\u00ae system. Extremity scans account for approximately 24% of all MRI scans performed today1. The expanded labeling now includes extremity scans using \u201cDetachable Upper and Lower Extremity Transmit\/Receive Coils.\u201d The expanded labeling is applicable to all previously implanted Axonics devices. \u201cThese additional … Continue reading "Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling"\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-20T10:03:06+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&sty=20210520005152r1&sid=flmnd&distro=nx&lang=en\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/axonics-receives-fda-approval-further-expanding-mri-labeling\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/axonics-receives-fda-approval-further-expanding-mri-labeling\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling\",\"datePublished\":\"2021-05-20T10:03:06+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/axonics-receives-fda-approval-further-expanding-mri-labeling\\\/\"},\"wordCount\":423,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/axonics-receives-fda-approval-further-expanding-mri-labeling\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/cts.businesswire.com\\\/ct\\\/CT?id=bwnews&sty=20210520005152r1&sid=flmnd&distro=nx&lang=en\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/axonics-receives-fda-approval-further-expanding-mri-labeling\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/axonics-receives-fda-approval-further-expanding-mri-labeling\\\/\",\"name\":\"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling - 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(Nasdaq: AXNX), a global medical technology company that is developing and commercializing novel products for the treatment of bladder and bowel dysfunction, has received FDA approval allowing the use of detachable extremity coils for patients undergoing 1.5T and 3.0T MRI scans. The FDA previously approved 1.5T and 3.0T MRI conditional labeling for using head and full-body transmit coils for the implantable components of the Axonics r-SNM\u00ae system. Extremity scans account for approximately 24% of all MRI scans performed today1. The expanded labeling now includes extremity scans using \u201cDetachable Upper and Lower Extremity Transmit\/Receive Coils.\u201d The expanded labeling is applicable to all previously implanted Axonics devices. \u201cThese additional … Continue reading \"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/","og_site_name":"Market Newsdesk","article_published_time":"2021-05-20T10:03:06+00:00","og_image":[{"url":"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&sty=20210520005152r1&sid=flmnd&distro=nx&lang=en","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling","datePublished":"2021-05-20T10:03:06+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/"},"wordCount":423,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/#primaryimage"},"thumbnailUrl":"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&sty=20210520005152r1&sid=flmnd&distro=nx&lang=en","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/axonics-receives-fda-approval-further-expanding-mri-labeling\/","name":"Axonics\u00ae Receives FDA Approval Further Expanding MRI Labeling - 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