Stryker Corporation Receives FDA Clearance for Innovative Incompass Total Ankle System

Reuters

06-25

Stryker Corporation Receives FDA Clearance for Innovative Incompass Total Ankle System

Stryker Corporation has announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Incompass® Total Ankle System. This new implant is designed for patients with ankle joints damaged by severe rheumatoid, post-traumatic, or degenerative arthritis. The Incompass system integrates advanced technologies from Stryker's existing Inbone® and Infinity® systems into a comprehensive solution for total ankle replacement. Developed using the Stryker Orthopaedic Modeling & Analytics (SOMA) platform, the system offers improved surgical flexibility and efficiency, leveraging data from extensive clinical cases and CT scans.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Stryker Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 20250625296275) on June 25, 2025, and is solely responsible for the information contained therein.

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Stryker Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 20250625296275) on June 25, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"GB00B4QBRK32.GBP","symbol_name":"FUNDSMITH EQUITY \"R\" (GBP) INC","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250625:nNDL5TlScl:1","article_id":"2546746217","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2546746217","pubTimestamp":1750853722,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Stryker Corporation has announced that it has received U.S. Food and Drug Administration  510 clearance for its Incompass Total Ankle System. 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This new implant is designed for patients with ankle joints damaged by severe rheumatoid, post-traumatic, or degenerative arthritis. The Incompass system integrates advanced technologies from Stryker's existing Inbone® and Infinity® systems into a comprehensive solution for total ankle replacement. Developed using the Stryker Orthopaedic Modeling & Analytics (SOMA) platform, the system offers improved surgical flexibility and efficiency, leveraging data from extensive clinical cases and CT scans.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Stryker Corporation published the original content used to generate this news brief via Business Wire (Ref. 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