Thanks, Marissa. Good afternoon, and thank you for joining us. For today's call, I'll provide a business update, and Anshul will provide additional detail regarding our financial results. Before I cover our record third quarter results, let me provide an update on recently published CMS Final Rule for calendar year 2023 Hospital Outpatient and ASC payments. On November 1 2022, CMS posted the calendar year 2023 rule for hospital allocations and ASC payments. Based on the final rule, calendar year 2023 facility reimbursement for minimally invasive SI joint fusion procedures performed in ASCs and hospital outpatient settings will increase by approximately 26% to $17,109 and 33% to $21,898 respectively. Today, 80% of our minimally invasive SI joint procedures are performed in an outpatient setting or at surgery centers. As these procedures continue to move to ASCs, the higher reimbursement in 2023 could potentially serve as a tailwind to demand and also allow us to maintain our pricing and sites of service. Now moving to our performance in the third quarter of 2022. I am very pleased with our strong execution, which resulted in record revenue driven by continued acceleration in procedure demand and robust surgeon interest in our portfolio of solutions. In the third quarter, we generated worldwide revenue of $26.4 million reflecting approximately 19% growth, compared to the third quarter of 2021 and 3% growth compared to the second quarter of 2022. In the U.S. our revenue grew 21% compared to the prior year period to a record $24.6 million. This revenue was driven by 25% US procedure volume growth in the quarter, a continued increase in our U.S. procedure volumes throughout 2022, while the healthcare systems continue to adjusting the staff limitations reflects strong demand for our solutions. In addition to accelerating top-line growth, we gained operating leverage across our organization as our revenue growth significantly outpaced operating expense growth, alongside the material sequential reduction in cash outflow in the quarter. With reimbursement tailwinds, expanded indications and strong surgeon engagement across our differentiated product portfolio, I am very excited about the potential to further accelerate growth. Our strategic investments and scalable infrastructure over the last few years provide a strong foundation to the core top-line growth and drive incremental operating productivity as we get into 2023. Now, let me provide an update on our key initiatives as we look to expand our leadership position and drive strong long-term growth. Starting with our sales infrastructure, our dedicated sales force remains an important driver of growth as we expand our core markets and grow our presence in trauma and adult deformity. Our sales force at the end of the third quarter included 85 territory managers and 72 clinical support specialists. With an increasingly seasoned sales force, our average trailing 12 month revenue per territory manager could increase by more than 10% since the start of the year. With our expanded portfolio, we are leveraging our growing distribution network for case coverage and selectively evaluating confinement strategies in hospitals. We are confident that this hybrid approach will complement our territory manager efforts and create additional capacity to drive surgeon engagements, ensure high quality support for our surgeons, and continue to deliver strong, and consistent top-line growth. Moving on to surgeon engagements, we ended the third quarter with a record active surgeon base of over 800 surgeons. This equates to approximately 27% growth in our active surgeon base over the comparable period in 2021 and approximately 12% growth sequentially. We’ve now seen seven consecutive quarters of double-digit year-over-year growth, which is a testament to our focused execution and education and outreach over the last several years. Surgeon adoption is one of the best leading indicators of long-term procedure demand. Additionally, we continue to experience a growing surgeon overlap across our various products. For example in 2022, over half of our active surgeons who performed in adult deformity procedure, also performed a minimally invasive SI joint fusion procedure using our solutions. We expect higher surgeon utilization as the synergistic surgeon base continues to grow over time. With the trauma indication expansion for iFuse-TORQ and the launch of iFuse Bedrock Granite, we are continuing to invest in surgeon indication to drive engagement and activation. We’ve also experienced a steady increase in the adoption rate of surgeons who have been trained on the simulator, which remains a valuable component in our certain training programs. Moving forward, we’ll continue leveraging our simulator training along with in-person local training and regional training to drive cost-effective surgeon engagement. We continue to expand our academic programs to educate residents and fellows. Since inception of the program, we've held training events in approximately 200 academic facilities in the United States and trained approximately 1,200 surgical residents and fellows. We are also expanding our trainings into new academic centers as we’ve seen a growing interest in our products among surgeon educators in new facilities. Education on Bedrock and iFuse Bedrock Granite in deformity are now integral to each training and we're adding content on iFuse-TORQ for our traumic locations. We are encouraged by the increase we are seeing in adoption by previously trained residents and fellows as we start practicing. Year-to-date, the number of fellows and residents who have completed a first case has more than doubled compared to this time last year while their procedure volumes have increased four-fold. Turning to products and solutions, our focused execution has resulted in nearly 3,000 surgeons worldwide performing over 75,000 procedures since the inception of the company. Expanding our platform of sacral pelvic solutions to address SI joint pain, spinal pelvic fixation and pelvic trauma has been a key tenet of our strategy and we’ve made substantial progress on this mission year-to-date. With iFuse-3D, iFuse-TORQ, and now iFuse-Bedrock Granite, we believe there is some value of our innovative, versatile, and complementary product portfolio provides surgeons with a comprehension set of alternatives and positions us with vast choice for surgeons who take our pelvic solutions. iFuse-TORQ continues to exceed expectations with another quarter of record revenue. iFuse-TORQ has been an important addition to the portfolio and provides a complementary action to iFuse-3D for our existing surgeons. It has been a valuable asset to convert users a competitive screw system. In trauma, while preliminary, we are seeing an uptick in the application of iFuse-TORQ to treat sacral fragility fractures based on the FDA expanded clearance in June. There are approximately 120,000 of these injuries per year in the United States. Most of which are currently not treated surgically. The fragility fracture market is a recognized unmet clinical need, hence our strategic importance to us as the sacral pelvic solutions leader. Over 75% of patients with fragility fractures are currently treated with Bedrock with a high cost for rehabilitation and involving significant complication deterioration in overall health status in many cases and a 25% one year mortality rate. In addition, orthopedic trauma surgeons, many fragility fracture patients are seen by our spine surgeons. We continue to invest in surgeon training and instruments re-confinement opportunities as we build out the trauma business which we believe will be an important avenue for growth over the long-term. In September, we also received FDA clearance for iFuse-TORQ to include fusion in conjunction with spinal pelvic fixation. Considering the successful launch of iFuse-Bedrock Granite, this expansion was important as it allowed iFuse-TORQ to complement iFuse-Bedrock Granite and the second point of fixation of the joints in the sacral alar iliac trajectory, which from a biomechanical perspective is important to attain fusion. We are excited about the success of iFuse-Bedrock Granite driven by strong surgeon interest in adopting the product and making it a standard-of-care for stabilizing the base along construct in adult deformity procedures. This was highlighted at a recently conducted Spinal Pelvic Think Tank Meeting in San Diego. The meeting was hosted by Dr. David Polly from the University of Minnesota, Dr. Greg Mundis from Scripps and Professor Jean-Charles Le Huec from Bordeaux University and attended by approximately 20 leading spinal deformity surgeons. We are pleased with the uptake of Granite despite our early stage in launch cycle. Additionally, Granite is providing a significant pull-through opportunity for the overall portfolio, as some surgeons are using some combination of our product to at least two points of fixation across the SI joint on either side resulting in a higher procedure average selling price. Given the positive experience with iFUSE-Bedrock brand, we’ve seen surgeons expand the use of the product to stabilize the base of shorter multi-level construct used in procedures to treat degenerative spinal conditions. Approximately, one-third of our iFuse-Bedrock Granite cases have been used in two to four level procedures. There are approximately 100,000 short construct procedures to the pelvic per year in the United States. Based on expanded use of iFuse-Bedrock Granite in short construct for certain patients this specifically results in an exciting opportunity for us to further expand our total adjustable market. Given the broad spinal deformity surgeon demand and support for iFuse-Bedrock Granite, we continue to successfully work with major hospitals across the U.S. to get the product on the approved list. This process, which is typically for new and highly differentiated products can take anywhere from few days to few weeks to complete depending on the procedure. We’ve also been working with our suppliers to optimize the workflow and address the challenges with near-term delays in adequate availability of implants. While the team is making significant progress on these workflows, both of these factors limited our ability to fully capitalize on the demand momentum in September and into the first half of the fourth quarter. On the clinical research front, in September, we enrolled the first of the targeted 120 patients on a SAFFRON study. As a reminder, this SAFFRON study is a prospective, randomized controlled trial of surgery using our iFuse-TORQ device versus non-surgical management in patients with debilitating sacral fragility or insufficiency fractures. We anticipate results to be available in late 2024. Talking about our patient awareness initiatives, in the third quarter we continue to see high website traffic, robust patient engagement, surgeon referrals and our Find A Doctor Locator metrics, while our cost of acquisition steadily declined. We use the Find A Doctor metric is a leading indicator of patient engagement and potential future demand. As a reminder, these outreach programs are targeted at patients in chronic, severe SI joint pain who are willing to service care for an extended period. Our goal is to connect patients with surgeons in their area who perform minimally invasive SI procedures using our product. Before I turn it over to Anshul, I'd like to provide an organizational update related to an addition to our international leadership team. In September, we appointed Neville Lorimer as the Vice President of International. Neville joined us from Conmed where he was a General Manager of the UK and Ireland and have 20 years of experience in the healthcare industry including over a decade at Stryker. Neville’s experience across orthopedics, spine and trauma will allow us to stabilize and grow our business in Europe, expand our international franchise and further accelerate top-line growth. I'll now turn the call over to Anshul to provide more detail on our financial results.