Thursday, April 03, 2008 10:58:01 AM
I'm wondering if Dean is able to offer some insight on this recent development?
One question that I have pertains to the progress that was made towards satisfying the FDA during their 9 month evaluation? Are they 80% to 90% satisfied? How much additional documentation is needed to completely satisfy the FDA, and the time factor involved?
Can the I3 team, along with the IDE studies, provide this data regarding "clinical imagery and functionality" to the IDE investigator in an expedited manner? Also, how many IDE sites will be involved and does I3 have Dominions available for the submission of this additional documentation to the FDA?
I'm long IMGG and have complete confidence in Dean & Company. However, I think it's good for everyone to have a better understanding in this uncharted terrority.
Thanks,
Glidelogic Corp. Becomes TikTok Shop Partner, Opening a New Chapter in E-commerce Services • GDLG • Jul 5, 2024 7:09 AM
Freedom Holdings Corporate Update; Announces Management Has Signed Letter of Intent • FHLD • Jul 3, 2024 9:00 AM
EWRC's 21 Moves Gaming Studios Moves to SONY Pictures Studios and Green Lights Development of a Third Upcoming Game • EWRC • Jul 2, 2024 8:00 AM
BNCM and DELEX Healthcare Group Announce Strategic Merger to Drive Expansion and Growth • BNCM • Jul 2, 2024 7:19 AM
NUBURU Announces Upcoming TV Interview Featuring CEO Brian Knaley on Fox Business, Bloomberg TV, and Newsmax TV as Sponsored Programming • BURU • Jul 1, 2024 1:57 PM
Mass Megawatts Announces $220,500 Debt Cancellation Agreement to Improve Financing and Sales of a New Product to be Announced on July 11 • MMMW • Jun 28, 2024 7:30 AM