Vivos Inc (RDGL)

[MikeD]

Since jhu vet school completed phase 1 containment tests meeting fda requirements as reported on rdgl blog, what if these containment results were than submitted already to fda by rdgl, to go along with the already fda submitted pre ide documents and the fda set the meeting up to go over the semantics of the human trials with the mayo clinic involved due to the ide approval being a foregone conclusion? Is that too much of a stretch of things or missing any steps?