Brad Mason
Analyst · SunTrust. Please go ahead. Your line is now open
Thanks, Mark, and good afternoon, everyone. As usual, I'll start by giving you a summary of our fourth quarter and full-year 2018 performance; after which, Doug will discuss the financial results more in-depth; I will then follow up with our outlook for 2019 and a few comments about my decision to retire before taking questions. In the fourth quarter, we recorded net sales of $121.1 million, representing a year-over-year increase of 3.6% or 4.4% in constant currency. Reported net sales for the full-year was $453 million, which was an increase of 4.4% year-over-year and a 3.9% increase in constant currency. As a reminder, revenue recognition accounting standards changed at the beginning of 2018, which impacted the year-over-year comparison to sales. When recasting Q4 2017 and the full year 2018 to the new accounting standards, net sales would've increased by 9.5% in Q4 and 5% for the full year in constant currency. Orthofix Spine, which includes our Bone Growth Therapies, spinal implants, Biologics, and Spinal Kinetics product lines generated $93.8 million in sales in the fourth quarter, which represents a 6.9% increase over prior year. Orthofix Spine produced $346.6 million in reported sales for the full year, a 4.8% increase over prior year. Beginning with Bone Growth Therapies reporting segment, this business continued its multi-year run of outstanding performance by delivering a net sales increase of 6.1% in the fourth quarter versus prior year. Despite our market-leading share, we continued to significantly outgrow the spinal fusion procedure growth rate, primarily through the continued adoption of our therapy by both existing and new customer physicians. In spinal implants, we reported a fourth quarter net sales increase of 17.9% compared to prior year, which reflects an increase in sales of 1.4% in spine fixation for the quarter and $3.59 million contribution from Spinal Kinetics. In spine fixation, U.S. sales returned to modest growth and sales from Spinal Kinetics were in line with our expectations for the quarter. For our Biologics business unit, reported sales decreased by 4.8% in the fourth quarter compared to prior year. The sales in this business continued to be negatively impacted by the contractual reduction in the marketing service fee Orthofix receives from MTF Biologics, which occurred in March of 2018. When normalizing for this change, sales increased 2.7% in the quarter, driven by increase of 4.7% in Trinity volumes, partially offset by a low single-digit ASP decline. Lastly, in our Orthofix Extremities, reported and constant currency net sales decreased 6.4% and 3.6%, respectively, in the fourth quarter over the prior year. When recasting Q4 2017 to the new accounting standard, reported net sales increased in the quarter by 13.2% and 16.6% in constant currency. Given this significant quarterly variability, we believe the best way to assess this business is to look at the constant currency year-over-year growth for the full year using the same accounting standard for both years. On this basis, Orthofix Extremities business grew 4.7% for the full year 2018. Moving on to non-sales metrics, our results reflect continued performance improvement in nearly every aspect of our business. For the fourth quarter, adjusted EBITDA as a percentage of net sales, excluding the impact from Spinal Kinetics, was 22% compared to 20.8% in the prior year period, a 125 basis-point increase. Adjusted earnings per share was $0.55, compared to $0.52 in Q4 2017. Excluding the dilution of Spinal Kinetics, adjusted EPS increased 19.2% over prior year. Free cash flow was $16.6 million for the fourth quarter, a $9.6 million decrease over prior year. This year-over-year decrease was primarily due to a favorable insurance settlement in Q4 2017. Adjusted trailing 12-month ROIC was 11.7% compared to 12.5% in 2017. When excluding Spinal Kinetics, adjusted ROIC was 15.5%. And lastly, we had a total cash balance of $72.2 million as of December 31, 2018. And for the full year, adjusted EBITDA as a percentage of net sales excluding Spinal Kinetics was 20.5% compared to 18.8% in the prior year period, a 170 basis-point improvement. Adjusted earnings per share was $1.79, compared to a $1.62 for 2017. Excluding the dilution of Spinal Kinetics, adjusted EPS increased 21% over prior year. And finally, free cash flow was $34.7 million for the full year which is a $12.6 million increase over prior year. Looking beyond the numbers, 2018 proved to be an important year for Orthofix. We moved our corporate domicile from Curaçao to Delaware, and reduced our long-term projected tax rate from 38% in 2017 to 27% in 2019. We also realigned our spine business segments to accelerate growth. And in our business development activities, in addition to acquiring Spinal Kinetics, we remained active yet disciplined. Regarding Spinal Kinetics, we’re very excited about our recent FDA premarket approval or PMA of the M6-C artificial cervical disc. If I think back over the history of Orthofix, few if any milestones were strategically important to the Company's future as the Spinal Kinetics acquisition last year and this approval. The M6-C artificial cervical disc is a next-generation artificial disc developed to replace an intervertebral disc damaged by cervical disc degeneration. Designed to restore physiologic motion to the spine, the M6-C disc is indicated as an alternative to cervical fusion. It preserves motion by restoring biomechanical function at the treated level after native disc removal and potentially reduces subsequent degeneration of adjacent vertebral segments. The M6-C device is the only artificial cervical disc that mimics the anatomic structure of a natural disc by incorporating an artificial visco-elastic nucleus and fiber annulus into its design. Like a natural disc, this unique construct allows for shock absorption at the implant level, as well as provides a controlled range of motion when the spine transitions in its combined complex movements. In fact, the M6-C disc is the only disc being marketed in the U.S with shock absorption capability and FDA approved labeling as such. As a reminder, the M6-C device received CE Mark approval for distribution in the European Union and other international geographies in 2006. And to-date, there have been more than 45,000 implants of the disc outside of the U.S. In addition to a full line of anterior, posterior and interbody fusion cervical implants, Orthofix offers the CervicalStim device, the only FDA-approved cervical bone growth stimulation therapy, and Trinity ELITE allograft, a market-leading stem cell allograft developed in partnership with MTF Biologics. With these products and now the M6-C disc, Orthofix has industry's most comprehensive and differentiated portfolio of cervical spine solutions. Regarding our launch plans, we expect some cases beginning in March performed by a few of our principal investigators followed by a controlled market launch late in the second quarter in the U.S. This plan includes an extensive training and education curriculum for surgeons and our sales representatives. The most important aspect of the launch is not how fast we go to market but how well we go to market. The M6-C disc will be a flagship product for Orthofix for many years to come. So, expect that we will do everything possible to assure that our surgeon customers and their patients have a great experience and outcome with every implant. In summary, 2018 was a year dedicated to position the Company for its next chapter. The FDA approval of M6-C disc marks the start of that chapter, a chapter that I believe will be the most exciting and rewarding since the Company's inception. With that, I’ll hand it over to Doug to give you more detailed financial results for the quarter and full year.