Reverse Stemless Total Shoulder starts clinical trial in the US

FX Shoulder USA, Inc. to Begin Clinical Study on Stemless Reversed Total Shoulder (press release)

FX Shoulder USA, Inc. will begin in December 2018 the FDA approved Investigational Device Exemption (IDE) clinical study of the Easytech Reversed stemless, a shoulder prosthesis, with its first implantation scheduled for December.

Easytech Reversed Stemless is an innovative shoulder arthroplasty implant that will be under clinical study with (9) sites and (12) surgeons across the U.S. participating. Building on the current success in France (home of FX Shoulder USA’s parent company, FX Solutions), where over 800 Easytech Stemless Reversed prostheses have been successfully implanted, FX Shoulder USA is slated to enroll patients at two (2) investigational sites in December and continue enrollment with additional sites beginning in January 2019.

“The Easytech Reversed may be exactly what the U.S. market is in need of, and a reversed stemless prosthesis could potentially be the future of shoulder arthroplasty,” said Baptiste Martin, CEO of FX Shoulder USA. “We are excited to begin our clinical study and enthusiastic to see the results with each successive case throughout. There is a lot of excitement among the surgeon investigators for Easytech Reversed,” he continued. In Europe, as per the article in Med Device Online dated April 11, 2018, stemless implants are projected to surpass stemmed implants by 2025.

Founded in 2011, FX Solutions has developed a large, unique and innovative range of prosthetic shoulder products, which include the Easytech Reversed Stemless. FX Solutions is now the second largest player in the French market, with more than 3,000 prostheses sold in 2018.

FX Shoulder USA, based in Dallas, Texas, is the direct provider of FX Solutions shoulder replacement devices in the U.S. FX Shoulder USA was founded in January 2018 and focuses exclusively on shoulder arthroplasty with a growing distribution network.  

http://www.fxshoulder.com/usa/

[email protected]

SOURCE FX Shoulder USA

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Surgeon wins $112,452,269 in royalties spat with Medtronic Spine

SPINE SURGEON WINS $112 MILLION IN ROYALTY BATTLE WITH MEDTRONIC (Orthopedics This Week)

An Indiana spine surgeon and inventor has prevailed in a five-year legal battle against medical device company Medtronic, with a jury awarding him $112 million in damages.

Rick Sasso, M.D., is a founding member and president of Indiana Spine Group and a board-certified orthopedic surgeon and a professor and chief of spine surgery at Indiana University School of Medicine, Department of Orthopaedic Surgery.

Sasso claimed that Medtronic violated contracts by not paying royalties on a pair of Sasso’s patented inventions: a spinal-implant system and a screw-implant system. Sasso sold the patents to Medtronic, but alleged that the company stopping paying him royalties, breaching its obligations and acting in bad faith.

According to Sasso’s complaint, his agreement with Medtronic provided for him to receive 2% of net sales on his inventions for a period of eight years. However, if a device was covered by a valid claim of a U.S. patent, then the royalty payments would continue for the life of the patent.

Sasso was the inventor of Medtronic’s Vertex system, which Sasso alleges is still covered by valid claims of numerous patents. Vertex has an estimated $200 million of sales in the United States.

Sasso also claims that Medtronic undercounted sales, not paying him royalties on numerous products that used Vertex components.

Following a month-long trial, a six-person jury returned a unanimous verdict in favor of Sasso. The jury awarded the spine surgeon $112,452,269, which is exactly the amount that Sasso requested.

Sasso’s attorney, Frederick Emhardt of Plews Shadley Racher & Braun, was pleased with the jury’s verdict. He wrote, “After a month of evidence, they learned much about spine surgery and the business of medical device sales and the need to honor contractual commitments, even if they were made by persons no longer with a company…. In a period of six hours, they unanimously rendered a verdict awarding to a dollar what Dr. Sasso requested—$112,452,269. The jury system is a bedrock of our way of life. It worked exactly the way intended by our founders.”

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Outlook for orthopaedics in 2019 – providing the best care at the lowest price

Cost of health care:Stethoscope money and smartphone

By focusing on improving outcomes – whether that’s through pre-operative management or more conservative care – at the lowest best price will help prove the value of orthopaedics in 2019 and beyond.

Providing the best care at the lowest price: Outlook for orthopaedics in 2019 (MedCityNews)

It is extraordinary how significantly medicine has evolved in past five years. We’ve gone from a time when private practitioners were combatively competing with hospitals, to hospitals realizing that they’ll struggle if they don’t adapt to the changing medical landscape as private practice groups have been forced to do in recent years. Now, we’re seeing that private practices and hospitals must work together to share resources to ensure the best health outcomes. And as we look at the next five years, there’s a good chance that procedures will move into outpatient settings whenever possible, putting even greater pressure on hospitals.

With healthcare costs consistently rising between five and a half and seven percent each year for the past five years, consolidation has been the standard in the industry. We’ve seen mergers like CVS/Aetna and UnitedHealth/DaVita working to control primary care, and big companies such as Amazon, Berkshire Hathaway and J.P. Morgan entering the space and moving the needle towards self-insurance. What’s been and what will continue to be the driving force behind consolidation and new industry players is robust data that confirms providers are who they say they are – proving that they are the best provider with the highest quality of care at the lowest price. That’s going to be the key factor moving forward, across healthcare and with orthopaedics specifically.

It is extraordinary how significantly medicine has evolved in past five years. We’ve gone from a time when private practitioners were combatively competing with hospitals, to hospitals realizing that they’ll struggle if they don’t adapt to the changing medical landscape as private practice groups have been forced to do in recent years. Now, we’re seeing that private practices and hospitals must work together to share resources to ensure the best health outcomes. And as we look at the next five years, there’s a good chance that procedures will move into outpatient settings whenever possible, putting even greater pressure on hospitals.

With healthcare costs consistently rising between five and a half and seven percent each year for the past five years, consolidation has been the standard in the industry. We’ve seen mergers like CVS/Aetna and UnitedHealth/DaVita working to control primary care, and big companies such as Amazon, Berkshire Hathaway and J.P. Morgan entering the space and moving the needle towards self-insurance. What’s been and what will continue to be the driving force behind consolidation and new industry players is robust data that confirms providers are who they say they are – proving that they are the best provider with the highest quality of care at the lowest price. That’s going to be the key factor moving forward, across healthcare and with orthopaedics specifically.

In the next year, I anticipate that orthopaedic physicians will be tasked with looking at total joint care by administering physical therapy more efficiently, decreasing readmissions and better preparing patients for surgery – with the overall goal of improving outcomes. Physicians will also be expected to manage the entire episode of musculoskeletal care – from the time a patient first complains of knee pain to surgery to the end of rehabilitation – while also driving efficiencies in cost.

The biggest question for the orthopaedics market in 2019 is whether a patient’s primary care doctor or orthopaedic specialist will serve as that care manager. That task is appropriately placed in the hands of orthopaedic specialists, but the race to see who will control the course of musculoskeletal care will be affected by several trends that I expect will dominate the orthopaedics market in the coming year.

Advancement of Value-Based CareIn 2018, we heard a lot of talk about value-based care, and I expect that trend will continue – if not exceed the pace — in the new year. However, value-based care will no longer just be about participating in and managing a structured program like bundled payments. Value-based care of the future will require providers to offer the best possible care, at the best price, with the best outcomes. How can you accomplish that? Two decisive factors for orthopaedic providers will be competitive data analytics and taking risks on total cost to control the course of care.

Obesity and The Rise of Bone DisordersOne of the least discussed topics in the orthopaedic market is the increasing incidence of bone disorders in the U.S. as a result of obesity. Two factors destroy knees: genetics, which you can’t control, and lifestyle choices, which you can change. Obesity astronomically raises the complication rate of routine surgery – in fact, it increases the risk of wound problems almost 10 times in obese knee and hip replacement patients. In 2019 and beyond, this will need to be addressed much more seriously by the orthopaedic industry – and we’ll need to spend a lot more time pre-operatively managing patients and not considering joint replacements until the patient can lose weight and demonstrate a healthy lifestyle. Pre-operative patient management will impact and improve outcomes, and lead to happier, healthier patients.

Spine ManagementIn the future of orthopaedic medicine, new data on best practices and management of musculoskeletal disease will likely prove what we already believe to be true – that we don’t deliver enough conservative care before we elect to operate. This will be particularly true for spine care. Because spine surgeons are so well-trained, many believe we should operate more often, and consequently there’s an overload of spine surgery in the U.S. – more so than any other country in the world. We don’t conservatively manage spine as well as we should, and as more data emerges, this is an area we’ll be able to improve.

Arthritis TreatmentArthritis is another area in the orthopaedics market where we can expect to see a change in the coming year. Arthritis is the leading cause of disability in the U.S., and estimates from the Arthritis Foundation say that nearly 54 million adults have doctor-diagnosed arthritis. With such a large number of patients seeking care for this condition, conservative treatment of arthritis is a clinical dilemma facing all orthopaedic specialties. Many new methods of regenerative medicine offer hope for conservatively managing arthritis in the future, and once we’re effective in doing so, we can considerably reduce the cost of musculoskeletal care.

By focusing on improving outcomes – whether that’s through pre-operative management or more conservative care – patients will be better cared for. At The Centers for Advanced Orthopaedics, we believe that will help us prove our value at the best price and with the best outcomes – and that’ll be the “name of the game” for the entire industry in 2019.

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Are you sure you have the right Notified Body?

Written by Joe Hage in the MedicalDevicesGroup on LinkedIn
 
You know that nice, little Medical Device Directive (the MDD) you’ve been using for 20 years to get a CE mark? You know it’s going away, right? Zero MDD certificates will be issued after May 25, 2020. And since CE marks need renewing every five years, by May 2025, everyone doing business in the European Union will have transitioned to the new way of getting their CE mark.
 
The new sheriff in town.
The Medical Device Regulation (MDR) is the new sheriff in town. He may be new, but he’s bigger and badder than his predecessor. You’re going to have to jump through some serious hoops to get your coveted CE mark. Or should I say, your notified body is going to have serious hoops to help you get your CE mark. Is your notified body (NB) up to the task? Are you in bed with the right partner?
 
Mark Schmark – How hard can it be?
I ignorantly thought, “Any NB worth its salt should be able to give a CE mark. Under this Directive, under that Regulation, whatever.” A CE mark is the basic requirement for marketing and selling medical devices in Europe. I mean, if a notified body can’t even give a CE mark for someone, how could they even be in business? Then I read Michelle Lott, RAC’s article.
 
Get your notified body on the phone. Like, now.
Michelle helped me understand these issues. Internalize them. 1. Are they designated? You don’t get to “just do MDRs.” Every notified body has to apply to become an MDR designee. Okay, that sounds pretty basic, right? If you’re in the NB business and you need one, you go get one, right? With a hat-tip to NSAI’s Colm O’Rourke for this data, 68 notified bodies have Withdrawn/Expired/Suspended Notifications to issue MDD certificates (so MDRs are terribly unlikely). Only 55 notified bodies even remain (see list) and, anecdotally, I hear fewer than half have even applied yet. 2. Have they been audited yet? Your NB has to weather a “Joint Assessment audit.” If they haven’t even scheduled one yet, get nervous. And if they had it – and it didn’t go well – get very nervous. 3. What did they apply for? Designations aren’t one-size-fits-all. Did your NB ask to cover your category of products? 4. Did they add staff? Michelle suggests – and a former TUV employee agrees – if your NB hasn’t added 20-30 percent to its payroll in the past three years, they won’t have the talent necessary to cover all the extra work. 5. How do they define “significant change?” This one’s a bit more nuanced. Basically, and whenever possible, you want your proposed product change to be considered “insignificant” by your NB. Because otherwise, you’ll need to apply for a new CE mark right away – and under the more burdensome MDR. Since each NB has its own interpretation of “significance,” you may find another NB has a looser definition, one that lets you squeak by without the added disruption.
 
In sum, you may have the wrong notified body if…

They haven’t applied for an MDR designation.
They haven’t scheduled a Join Assessment audit. Or they had one, and it went badly.
They didn’t apply to cover all your products, current and future.
They haven’t done some serious hiring in the past few years.
Their definition of “significance” is too strict.

I think Michelle’s article was super helpful in understanding this thorny issue. If you visit her site, you can download a copy of her Regulatory Pathways Assessment. It can help you work through project feasibility and requirements.
 
Coda: Can you afford to switch notified bodies?
I talked with Michelle afterward and pressed her. “Aren’t medical device manufacturers even lucky to have a notified body in the first place? I understand NBs are so busy and so under-staffed, they’re not even calling back new-business prospects in a timely way.” She quipped, “And if they can’t get you a CE mark, what’s the point of having them at all?” Touché. And drove home her point, “That’s why I’m telling all my clients to ask these questions. Because if your notified body is out of business, YOU’RE out of business.“

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How Orthopedic CEOs can navigate the coming Digital Disruption

How medical-device CEOs can navigate digital disruption in healthcare (McKinsey & Company)
Medical-device companies will need to reinvent themselves to stay competitive. Now’s the time to craft a strategy and scale a transformation.
Digital has already disrupted major sectors of the economy, and a revolution is underway in healthcare. As in other industries, battlegrounds are emerging, and there will be clear winners and losers. Medical-device players, facing unique opportunities and headwinds, will need to reinvent themselves as digital health companies to remain relevant and win in this fast-evolving market. Recognizing the urgency, almost all of the industry’s CEOs have declared digital health a top priority.
An earlier article, “Four keys to successful digital transformations in healthcare,” discussed broad trends and emerging battlegrounds—building direct relationships with consumers, finding new sources of value, collaborating for complementary capabilities, and contributing to burgeoning industry standards. Building on that work, this piece outlines how medical-device companies can define a winning strategy and design an at-scale digital transformation.
Where to start: Understanding stakeholder actions
Medical-device CEOs and boards recognize the power of digital and advanced analytics, and they’re investing in related capabilities. But for big changes to take hold and deliver lasting impact, they need to be woven into the organization’s DNA, including its culture and processes (for more questions to think about before a transformation, see sidebar “Preparing to win”).
Winning digital health companies will change in several ways at once: they’ll provide consistently delightful experiences to all customers, including patients, caregivers, clinicians, and providers. They’ll create a wide array of intelligent, personalized products that deliver demonstrable clinical value, and they’ll use insights on demand to take on appropriate risk with providers, payors, and regulators. They’ll also reimagine processes to dramatically reduce costs and accelerate decision making.
How do they get there? Rather than turn inward, we believe industry leaders should constantly evaluate the actions of stakeholders across the value chain to define the pace and direction of their responses in this frothy market, as shown in Exhibit 1.

 
Providers are scaling rapidly and making care delivery more sophisticated. Roughly 150 systems in the United States have established significant leverage and reach. They are vertically integrating to create clinical service lines that drive outcomes, manage risk, and create profit. Scale also allows providers to drive evidence-based medicine and create novel risk-sharing arrangements with manufacturers to control costs and improve outcomes.
Providers are also making the transition from offering B2B services to clinicians to B2C services for patients. As more clinicians are employed by hospitals, their ability to exercise their preferences is decreasing. In parallel, providers are moving beyond housing in-patient care to higher sources of value such as alternate-care settings and services, and monetizing assets, including data and patient access. All these changes have significant implications for medical-device companies’ innovation, offerings, services, and commercial models.
Payors are innovating while managing the bottom line. Those that have historically been viewed as B2B financial-underwriting entities are rapidly reinventing themselves as B2C organizations where members are a major source of revenue and digital is a critical capability.
For example, in the United States, led by the Centers for Medicare & Medicaid Services (CMS), payors are reducing costs through value-based programs. By 2020, CMS expects about 75 percent of contracts to be pay-for-performance. These changes are creating opportunities for innovative partnerships, raising the bar to demonstrate the value of products and services in real-world settings.
Policy makers are harnessing big data to assess safety and efficacy. In the United States, the Food and Drug Administration (FDA) is establishing a National Evaluation System for Health Technology (NEST) to “quickly identify problematic devices, accurately and transparently characterize and disseminate information about device performance in clinical practice, and efficiently generate data to support premarket clearance or approval of new devices and new uses of currently marketed devices. Essentially, NEST should be of, by, and for the medical device ecosystem and configured to provide maximal value to stakeholders, including the critical data needed by the FDA to make decisions that currently must be made with less comprehensive information.”1
This system brings together data from diverse sources and initiatives (for instance, PCORnet, Sentinel, registries, health plans, and delivery systems) to create a central mechanism to answer priority questions.
Each R&D organization will need to build new capabilities to succeed in this changing regulatory environment.
New entrants are flocking to healthcare. Large technology players and venture-capital-backed start-ups are bringing disruptive Silicon Valley mind-sets, speed, architecture, and investments at scale. Rather than posing an outright threat, tech companies offer healthcare incumbents many opportunities, as these companies are aware of their gaps in understanding of clinical and regulatory practices and are open to partnering with established healthcare companies (see sidebar “Examples of innovation”).
Imperatives for medical-device players
These changes across the value chain are collectively creating a “burning platform” that is compelling medical-device players to scale up their digital and advanced-analytics capabilities. Our cross-industry benchmarking tool, Digital Quotient, shown in Exhibit 2, demonstrates that digital capabilities are critical for performance, but medical-device and pharmaceutical companies’ capabilities are far behind those in other sectors.

To understand how to improve this dramatically, we analyzed the full spectrum of opportunities across the profit-and-loss statement of a typical medical-device company and identified more than 200 use cases. These can be organized in four broad themes.
Get closer to customers
As patients become more central to success, leading companies will need to understand, engage, and influence individuals better, just as the leaders do in consumer tech, retail, and consumer packaged goods.
Hospitals, who are customers for medical-device manufacturers, are also evolving. Winners will need to fine-tune their commercial engines to optimize their cost-to-serve and go-to-market models.
Example use cases:

Consumer engagement. Create a 360-degree view of patients connecting healthcare, environmental, and behavioral information to better understand what drives outcomes and to deliver timely, personalized microinterventions. We’ve seen players grow revenue by up to 10 percent using digital ecosystems that engage patients deeply.
Commercial-spend optimization. Optimize microtargeting to reach the right physicians and providers based on volumes, outcomes, risk profiles, purchasing behavior, and disease-incidence rates. In addition to lowering cost to serve by 15 to 20 percent, this approach identifies new customers to drive growth.

Build intelligent products and optimize the innovation engine
Winners will rethink all aspects of their models—offerings, go-to-market approach, and R&D operations—to capture new sources of value, drive efficiency, and compete in the changing market.
Example use cases:

Intelligent products and solutions. Wrap digital solutions around products to deliver better outcomes. These can span predictive diagnostics and early detection in imaging, fully digital operating rooms, and remote patient care in therapeutic areas such as cardiovascular, diabetes, and mental health.
Digital clinical trials. Optimize site performance by accelerating trial timelines and reducing costs, including better site selection, country footprints, and protocol optimization.

Assume more risk as appropriate
Winners will define novel risk-sharing relationships with providers. Some manufacturers have already begun to embrace new models of contracting (for example, early evidence in the bundled hip-and-knee markets), risk sharing (such as St. Jude Medical’s rebates for cardiac resynchronization therapies in case of required revision), and solutions (for example, Stryker’s subscription-based analytics packages) for providers. These require robust approaches to measure, track and underwrite outcomes in the real world.
Example use cases:

Value-based care. Collect and analyze data to track the total cost of care, patient outcomes, and patient satisfaction to develop creative manufacturer/provider contracting models. For example, a typical implant represents 15 percent of the total cost of the joint-replacement episode. Manufacturers are working with providers to optimize the remaining 85 percent (for example, inventory, operating-room utilization, and supplies).
Real-world evidence (RWE). Create a platform to collect, integrate, analyze, and report real-world data to prove treatment efficacy, safety, and value. Taking ownership of RWE can help create new markets, such as for 3-D mammography.

Reimagine processes
Reimagine and automate end-to-end processes to drive efficiency and unlock new insights. Federal healthcare agencies recognize this opportunity as well and have made important strides in their journey.
Example use cases:

Digital supply chain. Optimize supply-chain costs and improve customer service using data-driven insights into inventory levels and sales forecasts. A smart digital-inventory-management process helped a leading device player raise inventory efficiency by 15 percent.
General and administrative (G&A) automation. Digitize core G&A processes to create greater levels of efficiency and effectiveness. Leaders have captured 20 to 50 percent improvements in cost and efficiency.

Each of these changes has the potential to create significant value, and together, we estimate these advances can help leaders improve earnings by 15 to 30 percent. However, getting the full value of the opportunity will require embedding digital and advanced analytics in all aspects of operations, at scale.
How to design and execute a digital transformation at scale
The companies that succeed will move away from a bottom-up “let a thousand flowers bloom” approach and design a top-down at-scale transformation. The four keys for the transformation are shown in Exhibit 3.

 
All large healthcare companies are trying to transform themselves around these four keys. One such company is Johnson & Johnson, and its journey is described in an interview with its chief information officer, Stuart McGuigan. He talks about how the company decided to double down on the use of technology and build a flexible but secure digital IT organization supported by the cloud to enhance the development of smarter healthcare products and to improve customer and patient experiences with the company.
Several factors enable at-scale transformations such as the effort at Johnson & Johnson. These include clearly recognizing digital and analytics as a strategic priority and aligning the top team on themes for focus—for instance, intelligent products, customer engagement, and analytics on demand. It’s also important to invest in modernizing the IT foundation (for example, moving 85 percent workloads to the cloud or creating an enterprise-wide data foundation) and to stand up core enablers to manage the transformation (for example, reorganizing and hiring external talent, and developing an ability to launch and successfully manage every project as agile). Another key element is using the foundation to build value-creating innovations, such as through virtual enterprise resource planning, optical character recognition for technical blueprints, and tools to guide patients through the care journey and improve outcomes. We’re beginning to see the impact of these transformations and expect leaders to outpace their peers by wider margins in the next few years.
In addition to technical change, these transformations bring together the business and cultural aspects of managing large organizations. Six core concepts underpin successful at-scale digital transformations:

Agile @ scale. Dedicated business and technology teams come together to solve a specific problem in a matter of weeks.
Concept sprints for a minimum viable product. Cross-functional innovation workshops focus on seizing a specific business opportunity; in them, teams use design-thinking methodologies to quickly align on tangible solutions.
Data backbone. A scalable data backbone should establish a single authoritative source of critical information across the enterprise (for example, customer, product, pricing) and provide decision makers with business insights on demand.
Control tower. Out-of-the-box automated infrastructure oversees the overall program and tracks the progress of more than 50 teams in real time.
Value assurance. Teams are highly transparent and open to value audits; impact and return on investment are tracked on an ongoing basis, from inception to development and end-user adoption.
Culture change. A focus on winning the hearts and minds of all employees ensures they embrace the new way of working and adopt digital and advanced analytics in their everyday professional lives—just as they do in their personal lives.

Digital disruption is upon us in healthcare, and medical-device industry leaders are rapidly moving from pilots and experimentation to building real capabilities at scale. We believe our four-part architecture can help you ride this wave, improve patient outcomes, and create value for all stakeholders.

About the author(s)
Siddhartha Chadha is an associate partner in McKinsey’s New York office, and Sastry Chilukuri is a partner in the New Jersey office, where Steve Van Kuiken is a senior partner.

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