Wednesday, May 14, 2014 7:43:06 PM
So, roughly by this time next year, the following will be a reality:
1) Application for CE Mark to European regulatory agencies submitted
2) CE Mark approval from European regulators obtained
3) Limited commercial launch in Europe undertaken
4) Human trials in U.S. and final FDA approval submission process commence
As investors, I don't think we could have asked for more. If this is true, which we'll find out Wednesday, I apologize to Reiza and John for the snarky comments...
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