Gary L. Ellis
Analyst · Citigroup
Thanks, Omar. Third quarter revenue of $3,918,000,000 increased 2%, as reported, and 1% on a constant currency basis after adjusting for a $13 million favorable impact of foreign currency. While Physio-Control was part of Medtronic throughout Q3, we are treating it as a discontinued operation and our Medtronic revenue results do not include revenue from Physio-Control. Q3 revenue results, by region, were as follows: Central and Eastern Europe grew 28%; growth in South Asia, Latin America and the Middle East and Africa was 18%; greater China grew 12%; growth in our Western Europe and Canada region was 5%; Asia-Pacific grew 2%, including flat results in Japan; while the U.S. declined 3%. Emerging markets grew a combined 16% in Q3 and represented 10% of our total sales. It is important to point out that our results in greater China were negatively affected this quarter by the Chinese New Year, which fell in our Q3 this year while last year it was in our Q4. Accordingly, we would expect our greater China growth accelerate in Q4. Q3 GAAP earnings and diluted earnings per share were $935 million and $0.88, an increase of 1% and 2%, respectively. After adjusting for certain acquisition-related items, Physio-Control divestiture-related items, as well as the noncash charge for convertible debt interest expense, third quarter earnings and diluted earnings per share on a non-GAAP basis were $888 million and $0.84, a decrease of 4% and 2%, respectively. After adjusting for the onetime tax benefits we received in Q3 of last year, our non-GAAP diluted earnings per share increased 9%. In our Cardiac and Vascular Group, revenue of $2,029,000,000 grew 1%. Results were driven by growth in Endovascular and Peripheral, Structural Heart, AF Solutions, Renal Denervation, Pacing and Coronary, offset by declines in ICDs. CRDM revenue of $1,192,000,000 declined 3%. Worldwide ICD revenue of $674 million declined 9%, and we estimate that the worldwide ICD market declined in the low double digits. Despite the continued market slowdown on a year-over-year basis, we believe the U.S. ICD market is showing signs of sequential stability. In addition, the combination of our Protecta ICD, with its shock reduction and lead integrity alert technologies along with the long-term proven performance of our Sprint Quattro defibrillation leads, which are also now available with a convenience of a DF 4-connector, continues to perform well, both in terms of share and pricing. Pacing revenue of $467 million grew 3% in a market that declined in the low-single digits. Our U.S. Pacing business grew 8%, driven by the ongoing success of our Revo MRI SureScan pacemaker. Revo continues to command a mid-teens percentage price uplift, which is offsetting pricing pressure in the pacing market. Our AF Solutions business grew in excess of 40%, driven by the ongoing successful U.S. launch and the continued adoption in Europe of our Arctic Front cryoballoon. We are taking share in the AF market. Although we would expect more moderate double-digit growth in Q4 as we anniversary the U.S. launch of Arctic Front. Our Cardiovascular businesses had another strong quarter with revenue of $837 million, growing 8%, with 4% growth in the U.S. and 10% growth in international markets. Coronary revenue of $382 million grew 3%, and we maintained our #1 coronary stent position in markets where we had regulatory approval for both our Resolute Integrity drug-eluting stent and Integrity bare-metal stent. Worldwide drug-eluting stent revenue in the quarter was $195 million, including $37 million in the U.S. We were pleased to received FDA approval of Resolute Integrity late last week, which we believe will be a meaningful driver of revenue growth and significant share gains. To put the U.S. opportunity into perspective, in Europe, where Resolute Integrity is on the market and we have more competitors than in the U.S., our DES share is over double our U.S. share. Resolute Integrity is only – is also the only DES that has been approved for use in patients with diabetes, which is about 1/3 of the U.S. patient mix. In the international markets, we continue to take DES share due to Resolute Integrity's deliverability and clinical performance. In bare-metal stents, Integrity BMS allowed us to take another 3 points of share this quarter in the U.S. Turning to Renal Denervation, we continue to make progress on this multi-billion opportunity in hypertension and expect to generate $35 million to $40 million of revenue in FY '12. On the commercial front, we introduced our SYMPLICITY system into new centers in Europe and Latin America, and remain focused on expanding reimbursement into additional countries. We also continue to make progress in our U.S. pivotal study and are tracking towards U.S. approval in FY '15. Structural Heart revenue of $265 million increased 10%, driven by growth in transcatheter valves. We continue to split the TCV market with our competitor and have clear market leadership in transfemoral, the largest TCV segment. While the market in Europe was somewhat softer at the end of the calendar year, we continue to focus on deeper penetration in existing centers; access to new centers; new product introductions; and new access routes, including the subclavian and direct aortic approaches. Direct aortic had positive multicenter data at the STS conference and is becoming an attractive option for surgeons looking for an alternative to the transapical approach. We are seeing strong interest in our new 31-millimeter CoreValve, which treats a patient population that previously could not be treated by transcatheter valves. And we expect to expand our offering with CE Mark approval of our 23-millimeter CoreValve this spring. In the U.S., we are pleased with the progress of our CoreValve pivotal trial. Enrollment in the extreme-risk arm is complete and we continue to enroll these patients through continued access. We expect to finish enrollment in our high-risk arm this summer. Turning to Endovascular and Peripheral. Revenue of $190 million grew 17%. In the U.S., revenue growth of 25% was driven by the continued success of the Endurant abdominal stent graft. We have now anniversaried the launch of this product and would expect more moderate growth in Q4. Late in Q3, we received CE Mark approval for Endurant II, our next-generation AAA stent graft, which we expect will solidify our position as the market leader in the space. In peripheral, strong clinical data was presented earlier this month for our complete SE SFA, and we expect to receive an SFA indication in the U.S. later this summer. In drug-eluting balloons, we continue to post strong double-digit growth in Europe, and we continue to make progress on bringing this technology to the U.S. Now turning to our Restorative Therapies group. Revenue of $1,889,000,000 grew 1%. Growth was driven by solid performance in Surgical Technologies, Diabetes and Neuromodulations, offset by continuing challenges in Spine. Spine revenue of $784 million declined 10%. In core Spine, which includes core metal constructs, IPDs and BKP products, revenue of $596 million declined 6%. Core metal construct products declined 5%. The global core market remains challenged and slowed sequentially, with year-over-year growth now in the low-single digits. The U.S. market is also declining in the low-single digits, with mid-single digit pricing declines offsetting low-single digit procedure and mix growth. We have a number of initiatives underway to improve our performance, including the upcoming launch of POWEREASE, training surgeons on our new MAST MIDLF procedure, continuing to offer differentiated navigated spine surgery solution, as well as the continued rollout of Solera. While sales of Solera are growing at 10% and garnering a double-digit price uplift, we still have less than half of the total sets in the field today. However, we continue to roll out new sets including the 5.5, 6.0 larger rod diameters to treat complex spine and deformity, the portion of our product line most affected by competitive offerings. Over the coming quarters, we expect Solera to become over 40% of our core metal revenue mix, which should help to drive improvement in our spine performance. BKP revenues declined 7%. We have now posted sequentially flat results for 3 quarters in a row, which is relatively encouraging given the declines we have seen in this business over the past several years. In the U.S., we are seeing a modest uptick in BKP procedure volumes and our new products, including the recent launch of the Xpander 2, balloon appear to be stabilizing price. Biologics revenue of $188 million declined 20% in the quarter. BMP sales declined 26% in the quarter, including a 30% decline in the U.S. However, it is important to note that INFUSE is one of our lower margin products, muting its impact on our bottom line. Despite the increased pressure on INFUSE, we were encouraged to see double-digit growth in other biologics, including mid-teens growth in the U.S. We continue to see strong growth in our differentiated DBM offerings, including MagniFuse, a high-performance allograft formulation that was part of our Osteotech acquisition. Turning to Neuromodulation. Revenue of $419 million increased 4%, led by double-digit growth in neurogastro. In pain, we were pleased to receive FDA approval for the RestoreSensor spinal cord stimulator with our proprietary AdaptiveStim technology. We were unable to fully launch this product until the last week of the quarter due to a supply disruption resulting from the flooding in Thailand. This issue is now resolved and Q4 is off to a great start. We expect this breakthrough technology to drive growth and take share in the U.S. market. In DBS, we continue to see very little impact from competition in international markets and we saw strong double-digit new patient growth in the U.S. In neurogastro, the U.S. launch of InterStim Therapy for bowel control continues to go well and is contributing to the success of InterStim. Diabetes revenue of $367 million grew 8%, driven by double-digit growth in CGM. Our International Diabetes business grew 16% as we continue to see great adoption of our newest products in these markets. An example of this is our Enlite Sensor, which is driving very strong CGM growth in international markets, due to its improved comfort, accuracy and ease of use. Surgical Technologies revenue of $319 million grew 22%, including $31 million from our Advanced Energy business, which is the combination of our acquisitions of PEAK and Salient. Our integration activities continue to go well, and Advanced Energy is now a $120 million business, growing double-digits on a pro forma basis. Excluding Advanced Energy, Surgical Technologies had strong organic growth of 10%, with solid performances across all businesses. We delivered another good performance in capital equipment, led by our Fusion navigation system for image-guided surgery and the S7 surgical navigation system. In addition, we continue to see robust sales of disposables, especially in ENT power and monitoring. Turning to the rest of the income statement, I would like to note that my comments exclude the impact of Physio-Control. The gross margin was 76.2%, up 40 basis points from the third quarter of last year. While the gross margin did have a 30-basis-point benefit from FX, we continued to offset pricing pressure through our $1 billion cost of goods sold reduction program. We would expect our gross margin in Q4 to be in the range of 75.5% to 76%, which recognizes more of a negative impact from currency, as well as potential obsolescence of Endeavor, as we quickly ramp up the U.S. launch of Resolute Integrity. Third quarter R&D spending of $364 million was 9.3% of revenue. We remain committed to investing in new technologies and evidence creation to drive future growth, and expect R&D spending to be approximately 9% of revenue in Q4. Third quarter SG&A expenditures of $1,371,000,000 represented 35% of sales, which is a slight improvement year-over-year after adjusting for onetime executive separation cost last year. We expect Q4 SG&A in the range of 32.5% to 33% of revenue, which reflects the impact of several initiatives we are focusing on to leverage our expenses while at the same time investing in new product launches. Amortization expense for the quarter was $84 million compared to $86 million in the third quarter last year. For Q4, we would expect amortization expense in the range of $80 million to $85 million. Net other expense for the quarter was $67 million, flat compared to the prior year. Net losses from our hedging programs were $33 million during the quarter. As you know, we hedge much of our operating results to reduce volatility in our earnings. Net other expense this quarter also includes $21 million in expense from the Puerto Rico excise tax, which is almost entirely offset by a corresponding tax benefit I will discuss in a moment. Net other expense this quarter was favorable to our expectations, driven by lower than expected payments of spine royalties and the Puerto Rico excise tax as a result of slower end market volumes. Looking ahead, based on current FX rates, we anticipate Q4 net other expense will be in the range of $50 million to $60 million, including hedging losses in the range of $15 million to $20 million. Net interest expense for the quarter was $33 million compared to $70 million in the prior-year period. Excluding the $21 million noncash charge for convertible debt interest expense, non-GAAP net interest expense was $12 million. At the end of Q3, we had approximately $9.4 billion in cash and cash investments and $10.2 billion of debt. For Q4, we anticipate non-GAAP net interest expense will be in the range of $20 million to $25 million. Let's now turn to our tax rate. Our third quarter effective tax rate, as well as our adjusted non-GAAP nominal tax rate in the third quarter was 19.8%. Included in this rate is an $18 million tax benefit associated with the U.S. foreign tax credit from the Puerto Rico excise tax, which mostly offsets the charge recorded in other expense. Exclusive of onetime adjustments, we expect our FY '12 adjusted non-GAAP nominal tax rate in the range of 19.5% to 20%, which includes the tax credit associated with the Puerto Rico excise tax. Our Q3 GAAP results included a onetime deferred tax benefit related to the estimated gain on the sale of Physio-Control. It is worth noting that the timing of the tax benefit does not correspond to the timing of the sale gain which will be recorded in Q4, but will not impact our non-GAAP earnings. In Q3, we generated approximately $1 billion in free cash flow. We are committed to returning 50% of our free cash flow to shareholders. Fiscal year-to-date we have paid $769 million in dividends and repurchased $780 million of our common stock. As of the end of Q3, we had remaining authorization to repurchase approximately 75 million shares. Third quarter average shares outstanding on a diluted basis were 1,060,000,000 shares. In Q4, we have already started our share buybacks to offset the dilution from our Physio-Control divestiture and have bought back over $400 million thus far. Let me conclude by commenting on our revenue outlook and earnings per share guidance for the remainder of fiscal year 2012. This morning, we reiterated our revenue outlook and tightened our FY '12 earnings per share guidance. We believe a constant currency revenue growth rate of 1% to 3% remains reasonable. While we cannot predict the impact of currency movements, to give you a sense of the FX impact if exchange rates would remain similar to yesterday throughout Q4, then our Q4 revenue would be negatively affected by approximately $20 million to $40 million. Turning to our guidance on the bottom line. At this point in the year, we are comfortable tightening our earnings per share guidance range. We now expect FY '12 earnings per share in the range of $3.44 to $3.47, which after adjusting for $0.04 to $0.06 of dilution from the Ardian acquisition and $0.10 of onetime tax benefits we received in FY '11, implies FY '12 earnings per share growth of 7% to 8%. Based on our guidance, current FY '12 earnings per share consensus of $3.45 appears reasonable. As in the past, my comments on guidance do not include any unusual charges or gains that might occur during Q4, nor do they include the impact of the noncash charge for convertible debt interest expense. Finally, one housekeeping item. We will be hosting our annual institutional investor and analyst meeting this year on the morning of Friday, June 1. The meeting this year will be held in New York City. With that, Omar and I would now like to open the phone lines for Q&A. [Operator Instructions] If you have additional questions, please contact our Investor Relations team after the call. Operator, first question please.