Yes. I mean, we're held to really what CMS will release in terms of its final rule, which, as we know, just came out beginning of this month. We, as expected, work very closely with our installed base customers and specifically leading surgeons, or I should say, doctors, urologist, who are actively using our product and technology. So, as noted, when we had met with the HOP panel back in August, we obviously meant -- we weren't the only company that met with the HOP panel, but we had physicians with us shoulder to shoulder, as providers recommending the increases noted, moving to AP 6. And so, I think there's a strong clinical validation. I mentioned some of the data coming out and there's more and more data going on. There's more treatments going on. And so, I think, at this point, we can't influence the final rule, but we can continue the conversations with CMS in preparation for the review they'll do next year. And remember, these rulings come out on an annual basis. So, as mentioned, they'll start the process in the spring time. And we'll be involved directly with that process, all the way up until they announced the final rule for the forthcoming year. And I think, your -- to your questions in terms of supply chain or anything like that, I don't -- unless Marc has any comments, I don't see anything that has really disrupted us there. We talked about the San Diego sale and that sale was made and shipped in Q3. Unfortunately, it -- we had -- it wasn't out of our control, an issue with the transportation company and in route to the hospital. That is really what happened on that deal. That would have normally been recognized as a Q3 sale. So -- but it had nothing to do with COVID that I believe, that was just a mix up of transportation company. But, anyway, we're excited for continuing to progress, working with CMS, and we're using all available resources to make sure that we are well positioned for the next review.