lol I know. Not to insightful. However I’d ignore the noise of those saying this recent update about completing training next quarter means Vivos won’t submit IDE until then.
The previous update they already stated after they receive FDA approval to conduct clinical trials, they would complete final training for certification.
Here is part of the previous update, they posted.
“…After receiving FDA approval to conduct clinical trials we need formal approval from the Mayo Clinic IRB. In anticipation of this step and to help expedite the proccess we have submitted the Clinical Trial Protocol to their “gatekeeper” for comments. We have also been conducting certification training for Dr. Paz Fumagalli. Next quarter we are planning to complete the final training certification step using high activity RadioGel™ in a full-dress rehearsal operating theater.
So as I expect the last of the animal testing has been completed, final data write up and then IDE submission should be before end of Q1. JMHO.
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