FDA permits marketing of AI algorithm for detecting wrist fractures
fda.gov
fda.gov
My brother fractured his scaphoid bone during a high school lacrosse game, and the doctor who x-rayed his wrist did not detect it.
He continued living an active life with a broken wrist (he has a high pain tolerance) for several months before the worsening pain sent him to an orthopedic specialist.
Being unaware of the fracture, he had done quite a lot of damage to the bones in his wrist, which wound up needing multiple surgeries and nearly 18 months (!) in a cast to fully heal. He also permanenly lost a bit of that wrist’s range of motion.
I welcome any tool that helps doctors not miss this sort of thing!
Thankfully it wasn't broken at all, it just hurt like hell for a week.
The tech at the immediate care facility saw it, but my ortho didn't when he reviewed it on a follow-up. I had to point out the bone and where it was before my ortho saw it. His response was basically "Oops" followed by removal of the temporary cast/sling and replacing all of that with a reinforced removable brace (which was awesome, because I could easily shower).
I broke my hand after dumping my bicycle taking a corner too fast on a training ride (I was doing around 25 mph) and losing traction under my rear tire. Rode home about 5 miles on that broken hand...
For as long as he is alive, he will have less range of motion in his right wrist than his left, barring advances in nanotechnology bone reconstruction or something.
Millions of years from now, when his body has broken down into petrochemicals, I suppose that yes, his wrist will then have a greater range of motion then it does now.
But that’s hardly relevant.
If that is his attitude - and the attitude of everyone around him - then that will likely be the case.
In 'reality' - whatever that means to you - plenty of folks have demonstrated that the body is malleable.
With work, ROM is restorable.
A 510(k) requires demonstration of substantial equivalence to another legally U.S. marketed device. Substantial equivalence means that the new device is at least as safe and effective as the predicate.
A device is substantially equivalent if, in comparison to a predicate it:
has the same intended use as the predicate; and has the same technological characteristics as the predicate; or has the same intended use as the predicate; and has different technological characteristics and does not raise different questions of safety and effectiveness; and the information submitted to FDA demonstrates that the device is at least as safe and effective as the legally marketed device. A claim of substantial equivalence does not mean the new and predicate devices must be identical. Substantial equivalence is established with respect to intended use, design, energy used or delivered, materials, chemical composition, manufacturing process, performance, safety, effectiveness, labeling, biocompatibility, standards, and other characteristics, as applicable.
I would naively expect the bulk of new low risk ML product submissions to be de Novo submissions due to lack of real precedent.
Had the ER docs had this available I wouldn't have had to sit in agonizing pain and uncertainty for a day before getting into see a surgeon.
It wasn't wrist related, but it seems like the application of this to other stuff is not far off.
Very good news
Not sure why you think that, but I work in a similar field and I promise you you're wrong.