InvestorsHub Logo
Followers 15
Posts 2477
Boards Moderated 0
Alias Born 03/09/2017

Re: None

Wednesday, 01/13/2021 2:11:21 PM

Wednesday, January 13, 2021 2:11:21 PM

Post# of 106839
The skin graft example provided by the FDA was very weak. When we do tendon grafts we also dissect muscle tissue as tendons attach muscles to bones. The muscle tissue is not good for grafting purposes and is cut away from the tendon on a back table as part of the graft prep. In this process we alter the tissue as needed and then return it back to the patient in a different part of their anatomy (hamstring tendons used for ACL recon in the knee for example). The FDA has no oversight with autologous tissue related procedures.

When patients receive autologous blood transfusions (transfusions of their own blood) during surgery the blood recovered from suction is sent to a machine that cleans and then separates red blood cells from the fluid containing, fat, bone particles, and saline, and then returns scrubbed red blood cells back into the patient via transfusion. Again, the tissue, or in this case blood, is altered before being returned to the patient. And because it is blood products, there is no single destination within the body as blood circulates everywhere.

Personally, I think the judges have already made their minds up per the written brief previously provided and the hearing was mostly a formality. I expect them to send it back for trial. We will see.