I agree. There is no way I am seeing this as a negative. Nothing here was denied by the FDA. On the contrary. It seems that the FDA was requiring more info and trials due to not clearing 'back' (that was always my thought) and with this submitted neck trial and data, company feels that will be what the FDA needs to clear. And I do also. How many times have we gone back and forth with the FDA prior to getting foot and knee cleared. This IMO is not any different. And please, don't underestimate the power of having those two ALREADY CLEARED, for getting that FULL CLEARANCE eventually (or IMO soon). Due to the two products cleared, the FDA KNOWS the science. The FDA KNOWS the products are effective. The FDA KNOWS the products are safe. The FDA KNOWS the products ARE NEEDED (crisis).
Continuing communication between the two parties cannot be construed as anything but positive.