WebDEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Indications for Use Form Approved: OMB No. 0910-0120 Expiration Date: 06/30/ 2024 See … WebApr 10, 2024 · 510 (k) Premarket Notification. FDA Home. Medical Devices. Databases. A 510 (K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section 513 (i) (1) (A) FD&C Act) that is not subject to premarket approval.

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WebNov 17, 2024 · Sonex's first device, the SX-One MicroKnife ®, is FDA 510k cleared and is the first major technological advance in treating Carpal Tunnel Syndrome (CTS) in 20 years. WebMar 10, 2024 · You can send an eSTAR or eCopy to submit your 510 (k). After you submit your 510 (k) to the FDA, and when the FDA receives the 510 (k) submission, it assigns the … committee of 25

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WebSonex Health brings together a well-respected and experienced team of individuals who know how to create, develop and market medical technologies that can change the lives of millions of patients. Now, working as one, we’re tapping into the power of ultrasound guidance and innovation to transform the patient experience and improve healthcare. WebJan 14, 2024 · Barnes explained that Sonex Health’s mission is to be the leader in ultrasound-guided surgery and to equip physicians with therapies that reduce invasiveness, improve safety, and reduce the cost of care. Sonex Health provides the least invasive and safest way to perform carpal tunnel release surgery with the fastest recovery. WebMar 30, 2024 · Founded in 2014, Sonex Health’s mission is to be the world leader in ultrasound guided surgery by delivering physicians innovative therapies that reduce invasiveness, improve safety, and reduce ... dte energy near me shelby twp mi