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Hi ASH,

Can you confirm that and when the FDA application was lodged? The only reference I can find is in the prospectus on page 15 which states:

"A Request for Designation (RFD) to the US FDA to formally classify VitroGro� as a device is almost
complete. It is planned to submit this during April 2011 and based on advice from three well qualified
American regulatory consultants, the Board of Tissue Therapies believes that a formal device classification
should be received from the FDA by the end of June 2011."

I specifically noted at the time that they said "Planned" to be submitted during April. But I have not seen anything from the company to advise "When" it was actually submitted.

Not complaining but it would be nice to have this verified.

RE