Thank you, Jeremy. And good afternoon, everyone. I will start out today's call by reviewing our performance in the fourth quarter as well as providing additional insights around our key business priorities for 2025. Before turning the call over to our CFO, Rebecca Kuhn, to present the details of our financial performance for the quarter and year ended December 31, 2024, which will be followed by a Q&A session. Let's get started. 2024 was a tremendous year for the NeuroPace team as we delivered on several initiatives across our business. As a result, we grew total revenue in 2024 by 22% to $79.9 million compared to $65.4 million last year with contributions from sales of the RNS system and Dixie Medical SEEG products. The momentum in our business continued to rise steadily throughout the year and we reported record quarterly revenue in the fourth quarter. In addition, I'm very proud of our team's ability to consistently deliver this top-line growth while also effectively managing our gross and operating margins. Our forward-looking growth plans are focused on our three-part strategy of expanding adoption and utilization within level four comprehensive epilepsy centers, expanding site of service delivery with Project CARE, and expanding the indications of use for the RNS system. This strategy is designed to drive our near and medium-term growth plans across existing and new groups of clinicians as well as patients in the large total addressable market in the US. The first part of our strategy focused on increasing adoption and utilization of RNS systems in level four centers resulted in increasing the number of active prescribers of RNS therapy to record levels in 2024 and much of the RNS sales growth. Our core market opportunity within the level four comprehensive epilepsy centers is estimated at approximately $2 billion annually. We also made good progress throughout 2024 on expanding access to RNS therapy outside the level four CECs. We refer to this as the Project CARE program. The pilot program under this initiative was launched in early 2024. As we progressed throughout the year, we began to see an increase in the number of implants and referrals. Both the referrals and implant procedures began making a meaningful contribution to our revenue growth during the second half of 2024, a positive early trend with this program. We're executing these growth initiatives with financial discipline and have demonstrated gross margin improvement as well as efficient operating expense allocation, including investing in our organization, with a focus on our commercial team. The focus on these levers was demonstrated in 2024 by generating greater than 20% top-line growth while increasing operating expenses by only 7% and maintaining gross margins. However, these activities are just part of our long-range plan to drive growth. As we presented at our Investor Day in January, we are also advancing a number of key development programs across our clinical, product, and market development initiatives. With regard to clinical development, we've made good progress across three key programs: our post-approval study, and the Nautilus idiopathic generalized DRE and pediatric focal DRE indication expansion studies. We recently announced positive three-year safety and effectiveness data from our ongoing five-year prospective post-approval study of the RNS system, which is the largest prospective study in neuromodulation for adults with drug-resistant focal epilepsy. This strong data showed unmatched seizure control with lasting impact. Patients experienced rapid seizure reduction, long-term relief, and 42.5% of patients in the study experienced periods of seizure freedom for six months or more. These data are a great addition to the RNS system safety and efficacy profile and we can't wait to see the study data presented at AAN April 5th through the 9th, 2025. Moving to our ongoing Nautilus pivotal study, which I know everyone is really looking forward to seeing the top-line data in the coming months. As the first and only pivotal clinical study to evaluate neuromodulation therapy in the idiopathic generalized epilepsy or IGE population, if successful and supports regulatory approval, it would make the RNS system the first device-based therapy with an approved indication for idiopathic generalized epilepsy. In addition, this patient segment has the potential to have more ready access to RNS in that they do not require phase two invasive monitoring and would be able to proceed to RNS system therapy faster following a non-invasive diagnostic process that could be performed both within and outside of CECs. In terms of the status of the study, we expect the primary endpoint safety and effectiveness evaluations to be performed following the completion of one-year follow-up visits later this month. We will then plan to proceed with data readout and FDA submission in the second half of 2025. As also discussed in detail at our Investor Day, we are working on a pediatric indication for the RNS system as well with FDA and an organization called the National Evaluation System for health care technology, or NEST, an organization focused on the use of real-world data to expand indications for use, particularly to underserved populations. We believe RNS therapy for pediatric patients with drug-resistant focal epilepsy is a great candidate for this program. We are well underway on this initiative and are also working with the Pediatric Epilepsy Research Consortium or PERC on gathering an extensive set of data from a database we found with children treated with RNS therapy across 27 pediatric epilepsy centers and more than 25 peer-reviewed publications about RNS system use in pediatrics. These data have been the topic of several meetings with FDA to discuss how we can use all of these data sources to support an expansion in our indication for use. In addition, we have the support of several advocacy groups calling for the review. We believe that we are making good progress toward the attainment of the official NEST mark of approval. If this is the result, it would mean that the FDA has agreed in principle that the data is available to develop and support a full study protocol and they will accept that as sufficient. We would then perform a data analysis along with NEST following the protocol and provide that data to FDA. We also plan to submit these data to the FDA in the second half of this year. Moving to our product development programs in our annual cadence of product releases with AI-enabled software tools, remote programming, and our next-generation platform to enable efficiency, ease of use, and increased efficacy for the platform. As we continue to gather more and more data, we saw an exciting opportunity to use new cloud technologies to build the next-generation scalable patient data management system that will support our advancements into the future for years to come. And we plan to release our first AI-enabled software with an AI-powered seizure classifier that automatically identifies electrographic seizures. This has been designed to allow physicians an easier, more efficient path to treatment. In addition, physicians will be able to review histograms that show the progress of treatments as well as a patient's unique circadian and multiday rhythms. These are insights designed to translate directly to patient care. These are exciting developments, which we believe will further contribute to the access to and adoption of RNS therapy. As you can see, our team has been very busy in delivering on many fronts. And as I've mentioned previously, if you've not already had a chance, please listen to the archive of our Investor Day presentation held in January. It was a terrific event that offered some valuable insights from several KOLs and our own team members on many of the topics I discussed today. Considering the momentum in our business and exciting progress being made around each of our initiatives, we recently announced completing a public offering that we believe strengthened our balance sheet by the right amount, provided for potential increased liquidity of our stock, and allowed for organized evolution in our shareholder base. According to our recently presented long-range plan, we anticipate our cash and short-term investments will be sufficient to support our planned operations until achieving cash flow breakeven. As a result, we have terminated our ATM offering program. As I mentioned, in addition to raising capital to support our operations, as part of our recent offering, we raised approximately $49.5 million specifically to repurchase 5,270,845 shares of the company's common stock from KCK Limited, which was an early investor in NeuroPace. In this offering, we were able to bring in a strong new group of long-term focused investors while also providing an organized sale of all of KCK's remaining shares. We believe that this repurchase addressed the potential overhang on our stock that selling from KCK in the open market may have had in 2024. I would like to thank KCK for their support of NeuroPace over the years. We believe that the success of this offering demonstrated a strong interest in NeuroPace among new investors and support for our long-range plans. With that as an overview of our operational success in 2024 and goals for 2025 and beyond, let me now turn the call over to Rebecca to review our financial results for the fourth quarter of 2024 and guidance for 2025. Rebecca?