Thank you, Jee. Good afternoon. Thank you for joining Penumbra’s second quarter 2022 conference call. Our total revenues for the second quarter were $208.3 million, a year-over-year increase of 13.1% as reported and 15.3% in constant currency. Global vascular revenue grew 22.7% and global neuro revenue increased 1.5% compared to the same quarter a year ago. We expanded gross margins 180 basis points sequentially to 64.3%. We recorded non-GAAP operating income of $1.6 million or 0.8% of revenue in the second quarter. Looking forward, we expect to increase our revenue in the second half of the year and accelerate growth in 2023 with 4 significant catalysts, 3 major product launches and the presentation of significant clinical data. Sandra will also speak about these catalysts in a few minutes. Equally important in this economic climate, we expect to continue to expand gross margins with 70% plus as the goal within a few years, and we plan to increase operating profitability through discipline and operational improvements, notwithstanding the prevailing downturn in the macro economy. These catalysts which include both neuro and vascular, as well as our work on gross margins, and operating profitability will, I believe, make the next 12 to 18 months, one of the most robust eras ever for Penumbra. Turning back to the second quarter. I am proud of how our team executed, notwithstanding a very difficult operating environment, primarily in the United States. U.S. growth of 10.2% year-over-year was lower than we had anticipated and lower than we expect in future periods. The specific challenges most evident in our sector over the past few months included persistent staffing shortages, which challenged our hospital partners workflow, contract supply issues, which we think have receded, but are still watching in certain geographies around the world, and supply chain challenges which our team continues to address with success and resolve, but not without significant effort. These challenges were and still are evident, but we are getting better at addressing them. And we expect to further mitigate their impact in the second half of the year, during which we think growth in our U.S. business will accelerate. Our international business grew 20% year-over-year and is starting to reach scale. However, foreign currency fluctuations impacted our second quarter results and we expect FX to weigh on reported revenue in the second half of 2022 as well. Jason will address this later in the call. All of that said, the combination of our U.S. and international businesses and the 2 large areas neuro and vascular in which we participate, gives us a broad-based product portfolio and geographic platform to succeed in virtually any macroeconomic environment. Turning to our vascular business, we reported growth of 22.7% year-over-year to $123.5 million in the second quarter. We grew our vascular thrombectomy revenue of 30.3% year-over-year and our vascular embolization revenue of 11.8% year-over-year. Our U.S. vascular growth was driven primarily by increased utilization within existing accounts, who already believe in thrombectomy, but were early in the phases of trying our technology. This is in contrast with sales stocking in new accounts that primarily used lytics. In fact, based on our analysis, we believe we won competitively in both venous and arterial thrombectomy during Q2. While some of the macro factors that I discussed earlier clearly had an impact on our Q2 vascular growth in the U.S., we have seen a strong resurgence in the trends in our vascular thrombectomy business over the past month. Our current technology in venous and arterial disease, Lightning 12 and Lightning 7 represents a new treatment paradigm in both of these vascular anatomies, in which we have started to eliminate the typical tradeoffs in performing mechanical thrombectomy. Looking forward, we believe our 2 new vascular products, Lightning Flash and lightning Bolt will take us to another level of technology leadership in both markets. Lightning Flash introduces a new advanced catheter and incorporates a next generation Lightning algorithm that utilizes an extremely novel way to selectively control aspiration, which we think will increase the amount of clot we aspirate, further reduce the time it takes to do the procedure, and further optimize blood loss mitigation, while also reducing the risk of vessel lumen damage. Just as potentially important as Lightning Flash could be in the venous market, we are equally excited about the potential for Lightning Bolt in the arterial anatomy. Lightning Bolt is designed with an extremely sophisticated algorithm. The technology incorporates both dual pressure sensors inherent in our current Lightning algorithm that helps mitigate blood loss, as well as the clock extraction technology inherent and fundable for ischemic stroke, which I will discuss in a few minutes. Moreover, our team along with key opinion leaders are advancing significant clinical work and building proof that our proprietary innovations improve outcomes, reduce complications, and are advancing the field overall. We expect much more discussion of important clinical work at medical meetings going forward, as many physicians collect and present their experiences using our technology versus the competition. For example, at the recent VTE Summit in San Diego, independent data was presented on 85 DVT patients treated with current thrombectomy systems, including Lightning 12, which comparatively produce superior results. We look forward to the data and other independent datasets being presented, published and discussed going forward. Further, we expect presentation of the first 60 patients enrolled in our STRIDE PE trial at the PERT Symposium in October, which we think will highlight our position in the PE market. On the arterial side, we expect to finish enrollment in our STRIDE study by year-end with acute results expected to be presented next spring, which we believe will increase awareness and adoption of Lightening 7 and acute limb ischemia. In addition, Sandra will discuss 2 new randomized clinical trials that we plan to conduct in vascular thrombectomy in the near-term as well. In coronary, CAT RX continued to strong growth trajectory in the U.S., as did our vascular embolization business even though we did see an impact to the latter from the macro dynamics during the quarter. We also initiated a successful launch of both Lightning 12 and Lightning 7 in the European market. Moreover, the introduction of our original Indigo thrombectomy products into China was successful, and we expect strong growth going forward. We also are working toward an introduction of our vascular thrombectomy product into the Japanese market. Turning to our neurovascular business, our revenue grew to $84.8 million in the second quarter of 1.5% on a year-over-year basis, and 4.6% sequentially. Our U.S. stroke business grew strong double digits again year-over-year, while our neuro embolization and international stroke business offset this growth. We are excited to announce FDA approval of our IDE for the THUNDER trial, effectively starting the Thunderbolt era in stroke therapy. The excitement among the neurovascular community about this technology, and this trial is palpable. We expect enrollment to be brisk, and believe Thunderbolt could be launched in the United States in the second half of 2023. We have said it before and physicians who have now seen the Thunderbolt agree. This technology could completely change the paradigm in ischemic stroke treatment by both improving patient outcomes, as well as potentially allowing neuro physicians to treat more ischemic stroke patients safely, efficaciously, and expediently. Since the Thunderbolt trial is underway, this is an appropriate time to spend a few minutes explaining what Thunderbolt is and how it works. Thunderbolt is a microprocessor controlled advanced software algorithm integrated into the tubing that sits between the engine pump and the read catheter. It does not go into the patient’s body directly. Thunderbolt orchestrates modulating aspiration, which is proprietary to this technology. Two valves are integrated into Thunderbolt. One valve directly connects the RED catheter of choice, 62, 68 or 72, to our engine pump. The second valve connects the RED catheter to a non-pressurized saline bag. The Thunderbolt algorithms orchestrate the opening and closing of each valve up to 12 times per second once clot engagement is detected. This modulated aspiration disrupts the friction between the clock and the tip of the catheter. Eliminating this friction, we believe will allow the RED catheters to ingest the clot the vast majority of the time. This compares to the current practice with aspiration, which ingestion occurs a small percentage of the time, even with larger board catheters that are much more challenging to track to the clock. Because of this, we expect Thunderbolt to change another existing paradigm in interventional stroke. We believe it will allow doctors to use smaller catheters, while getting the unique benefits of modulating aspiration faster, more complete clot removal. This could have been added benefit of increasing the number of treatable patients by allowing for the routine treatment of more distal occlusions. In our U.S. stroke business, Thunderbolt is the clear priority. That said, we also expect to launch an additional RED catheter in the second half of the year, which we believe will be a very important addition to our market leading portfolio. We also expect to launch the RED catheter family into the European market during Q3, which will help us revitalize our European neuro business. I’ll now turn the call over to Sandra Lesenfants, President of our Interventional business, to give her perspective on our new product pipeline and clinical trial strategy.