this post was submitted on 26 Mar 2024
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@GottaLaff
Lots of questions
@mloxton We need lots of answers.
@[email protected]
I think I know the answer to the main question, and it is a bit boring.
I expect that Neuralink got approval for human testing because they used a "same as" application, and could cite many other very similar implants that had been previously approved for other applicants. (2002, 2006, etc)
I want to know how this patient selected, the end points, what is this "issue" that the patient mentioned, what outcomes and adverse effects are being monitored, what are the rollback options?