Skip to content

1st human has received Elon Musk’s Neuralink brain implant, billionaire says

Cbc :

The first human patient received an implant from Elon Musk’s computer-brain interface company Neuralink over the weekend, the billionaire says.
In a post Monday on X, the platform formerly known as Twitter, Musk said that the patient received the implant the day prior and was “recovering well.” He added that “initial results show promising neuron spike detection.”
Spikes are activity by neurons, which the National Institutes of Health describe as cells that use electrical and chemical signals to send information around the brain and to the body.
The billionaire, who owns X and co-founded Neuralink, did not provide additional details about the patient.
Neuralink is one of many groups working on linking the nervous system to computers, efforts aimed at helping treat brain disorders, overcoming brain injuries and other applications. There are more than 40 brain computer interface trials underway in the U.S., according to clinicaltrials.gov.
When Neuralink announced in September that it would begin recruiting people, the company said it was searching for individuals with quadriplegia due to cervical spinal cord injury or amyotrophic lateral sclerosis, commonly known as ALS or Lou Gehrig’s disease. Neuralink reposted Musk’s Monday post on X, but did not publish any additional statements acknowledging the human implant. The company did not immediately respond to requests for comment from The Associated Press or Reuters on Tuesday.
Neuralink’s device is about the size of a large coin and is designed to be implanted in the skull, with ultra-thin wires going directly into the brain. In its September announcement, Neuralink said the wires would be surgically placed in a region of the brain that controls movement intention.
The initial goal of the so-called brain computer interface is to give people the ability to control a computer cursor or keyboard using their thoughts alone. The company previously announced that the U.S. Food and Drug Administration had approved its “investigational device exemption,” which generally allows.