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Re: SC8 post# 145013

Sunday, 03/06/2022 5:17:17 PM

Sunday, March 06, 2022 5:17:17 PM

Post# of 173582
As for the EFS IDE process, to “market” the radiogel device is not to supply it for purchase as you stated but rather to simply move past the initial FDA EFS IDE approval process and on to human trials.

https://mdic.org/wp-content/uploads/2018/12/MDIC-EFS-Blueprint-for-EFS-Success-2016.pdf

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