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October 4, 2017 OrthoSpineNews

OrthAlign, Inc., a privately held U.S.-based medical device and technology company, received CE Mark Approval to market its advanced precision technologies for Direct Anterior Approach Total Hip (DAA HipAlign®) and Unicompartmental Knee Arthroplasty (UniAlign®) surgeries, in Europe and other countries.

“As OrthAlign has focused on expanding customer reach and its application pipeline in 2017, we are pleased that surgeons outside of the United States and Japan can now have access to our newest precision technologies DAA HipAlign and UniAlign,” said Eric B. Timko, OrthAlign’s Chief Executive Officer and Chairman. “We will continue providing orthopedic surgeons and healthcare facilities throughout the world our clinically beneficial portfolio of products, staying true to our core design principles of ease of use, precision, and cost effectiveness.”

Recent global statistics have shown that the direct anterior approach for total hip arthroplasty is growing, as it arguably leads to quicker recovery, less pain, and more normal function for patients after hip replacement. DAA HipAlign does not require any pre-operative imaging or intraoperative fluoroscopy, while providing more clinically relevant positioning for cup placement and leg length measurement. Early clinical data from the United States demonstrates that surgeons can expect to reduce fluoroscopy exposure time by about 45%. Early clinical data from Japan shows cup placement (for both inclination and anteversion) accuracy of ±10°, with at least 95.9% confidence.

Unicompartmental knee arthroplasty procedures are also growing in popularity, worldwide. UniAlign establishes the mechanical axis of the tibia, determining the varus/valgus angle and the posterior slope angle of the cutting block relative to the tibia, for the transverse resection. The system has been validated in simulated use testing to achieve resection accuracy of ±2.0° in the coronal plane, ±3.0° in the sagittal plane and ±2.0 mm in depth. This accuracy has been validated with at least 90% confidence.

“As international expansion has been one of OrthAlign’s priorities, receiving CE Mark approvals for use of our technology in two rapidly growing segments is great news,” said James Young Kim, OrthAlign’s Vice President and General Manager of International. “Our international distributor network has been waiting for these approvals, as many of their local surgeons have been asking for the technology.”

DAA HipAlign and UniAlign will be included in OrthAlign Plus® handheld navigation devices, along with OrthAlign’s award-winning KneeAlign® technology. To date, OrthAlign technology has successfully been used in over 65,000 cases, in over 25 countries, with more than 15 published international clinical studies demonstrating its accuracy.

About OrthAlign, Inc.

OrthAlign is a privately held medical device and technology company, developing advanced technologies that deliver healthier and more pain-free lifestyles to joint replacement patients, globally. We provide healthcare professionals with cutting edge, computer-assisted surgical tools that seamlessly and cost-effectively deliver vital data and clinical results to optimize outcomes for our patients. For more information regarding OrthAlign, please visit http://www.orthalign.com.

“ORTHALIGN®, ORTHALIGN PLUS®, KNEEALIGN®, KNEEALIGN® 2, HIPALIGN®, and UNIALIGN™ are registered trademarks of OrthAlign, Inc.”

 


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September 29, 2017 OrthoSpineNews

9/27/2017

Aliso Viejo, CA, Sept. 27, 2017 (GLOBE NEWSWIRE) — OrthAlign, Inc., a leading provider of orthopedic surgical navigation solutions, announced today that the company has raised $10 million in a series D financing round. The investment will be used to fuel product development as the company expands from a solution provider for total knee surgery to a platform technology provider for total knee, partial knee, and total hip replacement surgeries. The funds will additionally be used to support continued commercial expansion through investments in hiring and key programs both in the U.S. and International markets.

OrthAlign manufactures and distributes its core technology, KneeAlign®, which is a computer-assisted navigation application for total knee replacement surgery. KneeAlign has powered more than 65,000 surgeries worldwide, and is clinically-supported by more than 15 peer-reviewed published studies. KneeAlign is well positioned as a perfect solution for the future of orthopedic surgery, delivering the accuracy and consistency that users demand while avoiding the unnecessary capital and recurring costs that large-console navigation and robotics bring to the healthcare market. Reducing instrumentation trays and delivering information directly into the surgeon’s hands, the KneeAlign technology is the only computer navigation platform that exists 100% within the sterile field. These same fundamental benefits continue to resonate with expansion into Uni and Hip applications.

“We are pleased to have completed our latest financing round to support our operational goals of strong revenue growth and application expansion,” said Eric B. Timko, Chairman and CEO of OrthAlign. “We continue to invest in developing KneeAlign because we see it as a key component of the total knee replacement technology landscape moving forward, especially considering the importance of delivering solutions in the ambulatory surgery center environment. But we are no longer a single-solution provider, and have rapidly expanded our commercial platform technology to include solutions for partial knee replacement with our UniAlign™ application. Our solution for total hip replacement, HipAlign®, supports both posterior- and direct anterior approaches and is currently in a limited user release with full-commercialization slated for 2018.”

“We are truly excited for the next phase of OrthAlign,” said Gary Henley, board member. “With a new management team in place, the company’s focus on expanding commercial footprint domestically and in key markets around the world, coupled with a focus on research and development, position the business for long-term success in this competitive marketplace.”

This latest financing round was led by existing investors River Cities Capital Funds, California Technology Ventures, Research Corporation Technologies and Mutual Capital Partners who show continued support for the company.

ORTHALIGN, INC.

OrthAlign, Inc. is a privately held medical device and technology company, developing advanced technologies that deliver healthier and more pain-free lifestyles to joint replacement patients, globally. We provide healthcare professionals with cutting edge, computer-assisted surgical tools that seamlessly and cost-effectively deliver vital data and clinical results to optimize outcomes for our patients. For more information regarding OrthAlign, please visit www.orthalign.com or contact Adam Simone (asimone@orthalign.com).

 

 Adam Simone OrthAlign, Inc. asimone@orthalign.com


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September 28, 2017 OrthoSpineNews

FREMONT, Calif.Sept. 27, 2017 /PRNewswire/ — THINK Surgical, Inc., a global medical device manufacturer of the only active robotic surgical system for orthopaedic surgery, announces that it has entered the South Korean market with its TSolution One Surgical System and has successfully completed over ten Total Knee Arthroplasty (TKA) cases.

On Aug. 22, 2017, the first commercial TKA surgery using the TSolution One Surgical System was successfully performed by Dr. JongHo Park at Busan Centum Hospital in Busan City, Korea. Busan Centum is the first hospital in Korea to offer the TSolution One Surgical System, the latest robotic system for joint replacement. Since then, more than 10 cases have been accomplished between Dr. Park and his colleague, Dr. ChanMo Son. According to Dr. Park, “Pre-surgical preplanning was found to be effective in discovery of deformation on lower limb or joint. High-precision bone cutting reduces pain after surgery and improves functional recovery.” Both surgeons have recognized the benefits of active robotics for their patients and look forward to treating more patients using this exclusive technology.

The TSolution One Surgical System received clearance from the KFDA earlier this year. It received clearance for Total Hip Arthroplasty (THA) in February and TKA in March. The system currently has 510(k) clearance for THA in the U.S. and CE mark for use in the EU and plans to obtain 510(k) clearance and CE mark for TKA in the near future. The TSolution One core technology has been used in thousands of total joint replacements for both hip and knee worldwide.

“This milestone demonstrates how quickly TSolution One can be adopted in an OR environment. We truly believe it has the ability to transform joint replacement procedures to improve surgical outcomes and make difficult surgeries more predictable,” said John Hahn, CEO of THINK Surgical, Inc.  TSolution One is an open platform system that provides surgeons with CT based 3D pre-surgical planning using an open implant library combined with a surgical robot that precisely executes the patient’s personalized plan and prepares the bone cavity and joint surface with sub-millimeter dimensional accuracy.

About Busan Centum Hospital
Busan Centum Hospital opened on Dec. 2, 2002, in the heart of the East Busan, Suyounggu Gwangan-dong as an orthopedic surgical hospital and is committed to providing quick and accurate diagnosis and fast healing through cooperative treatment with several related hospitals. Centum Hospital always tries to provide patient-oriented medical service.

About THINK Surgical, Inc.
THINK Surgical, Inc. is committed to the future of orthopaedic surgery and to improving patient care through the development of leading-edge precision technology. THINK Surgical develops, manufactures, and markets the only active robotic surgical system for orthopaedic surgery.

For more information, visit www.thinksurgical.com.
TSolution One® are registered trademarks of THINK Surgical, Inc.

Contact: THINK Surgical, Inc.
510-249-2300
info@thinksurgical.com

Related Files

THINK Press Release_Korea_Final.DOC

SOURCE THINK Surgical, Inc.


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September 28, 2017 OrthoSpineNews

WARSAW, Ind.Sept. 11, 2017 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, today announced the launch of the Persona® Partial Knee System, the latest addition to its portfolio of personalized and anatomically designed knee implant systems. The launch of the Persona Partial Knee System is the first significant jointly developed new product for the Company since the Zimmer Biomet combination, and reinforces the Company’s leadership position in partial knee replacement.

“The global introduction of the Persona Partial Knee System is the combined Company’s first major product launch and fills a significant gap in our knee portfolio,” said Daniel Florin, Interim Chief Executive Officer, Senior Vice President and Chief Financial Officer. “The partial knee market continues to expand as patients demand alternatives to traditional knee replacement. The addition of the fixed-bearing Persona Partial Knee System complements the Company’s mobile-bearing Oxford® Partial Knee, further strengthening our leadership position in this growing market.”

The Persona Partial Knee System represents the next era in personalization, equipping surgeons with a comprehensive system of implants and instruments that are designed to offer an uncompromising fit and efficiency in the operating room. The development team leveraged global experts in partial knee replacement and utilized the ZiBRA™ Anatomical Modeling System to analyze thousands of bones, both male and female, representing a diverse global population.

“The new Persona Partial Knee System has made me a better partial knee surgeon,” said Craig Della Valle, MD, a developing surgeon from Rush University Medical Center in Chicago, Illinois. “Its combination of compartment-specific implants that fit better to ergonomic instruments has made me both more accurate and efficient. The system is definitely a move forward in the right direction,” said Dr. Della Valle.

Rocci Trumper, MD, at Poudre Valley Hospital in Fort Collins, Colorado successfully performed the first surgery of the Persona Partial Knee System since the full global commercial launch on August 31, 2017. “The instruments were thoughtfully designed and the tibial component fit well,” said Dr. Trumper.

There have been more than 1,000 cases to date across centers in the U.S., EMEA and Japan, and more than 260 patients have been enrolled in a 10-year global multi-center study.

“The introduction of the Persona Partial Knee System comes at a significant time as we continue to see an increase in the demand for knee replacements,” said Dan Williamson, Zimmer Biomet’s Group President, Joint Reconstruction. “This innovative technology furthers our commitment to restore mobility, alleviate pain and improve the quality of life for patients around the world.”

About Zimmer Biomet
Founded in 1927 and headquartered in Warsaw, Indiana, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic reconstructive products; sports medicine, biologics, extremities and trauma products; office based technologies; spine, craniomaxillofacial and thoracic products; dental implants; and related surgical products.

We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.

We have operations in more than 25 countries around the world and sell products in more than 100 countries. For more information, visit www.zimmerbiomet.com, or follow Zimmer Biomet on Twitter at www.twitter.com/zimmerbiomet.

Cautionary Statement Regarding Forward-Looking Statements
This release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.  Forward-looking statements include, but are not limited to, statements concerning Zimmer Biomet’s expectations, plans, prospects, and product and service offerings, including new product launches and potential clinical successes.  Such statements are based upon the current beliefs and expectations of management and are subject to significant risks, uncertainties and changes in circumstances that could cause actual outcomes and results to differ materially.  For a list and description of some of such risks and uncertainties, see Zimmer Biomet’s periodic reports filed with the U.S. Securities and Exchange Commission (SEC).  These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included in Zimmer Biomet’s filings with the SEC.  Forward-looking statements speak only as of the date they are made, and Zimmer Biomet disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.  Readers of this release are cautioned not to rely on these forward-looking statements, since there can be no assurance that these forward-looking statements will prove to be accurate.  This cautionary statement is applicable to all forward-looking statements contained in this release.

ZBH-Corp

SOURCE Zimmer Biomet Holdings, Inc.

Image courtesy of Zimmer Biomet.


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September 26, 2017 OrthoSpineNews

Paxeon Reconstruction, a manufacturer of best-in-class orthopedic products including derivative and emerging products, announces that Dr. Christian Christensen has completed a retrospective study that included 147 patients that underwent total hip arthroplasty in an outpatient surgery center.

Total hip arthroplasty has traditionally been performed in hospitals with a 3-5 day hospital stay. More recently, these surgeries have been done in outpatient surgery centers. These surgery centers have allowed higher levels of surgeon control and increased patient satisfaction. Performing traditionally inpatient procedures in an outpatient arena has allowed the opportunity for cost savings that can be shared by patients, surgeons, and surgery center owners. Cost savings are experienced by decreasing the length of facility stay and also by decreasing the material expenses associated with performing total hip arthroplasty.

Dr. Christensen of Lexington, Kentucky has compared the cost of performing total hip arthroplasty with a Paxeon product versus performing the procedure with both a Stryker and a Biomet product. Over a calendar year, these 147 cases were performed with a savings of more than $2,700 per Biomet hip and $1,040 per Stryker hip.

Since Dr. Christensen used the value based Paxeon product, an annual savings of over $400,000 per Biomet hip and over $150,000 per Stryker hip was realized. All hips were uncemented and included a ceramic head and a cross-linked polyethylene.

Kyle Sineath, President of Paxeon Reconstruction said: “We are thankful to Dr. Christensen for bringing to light the fact that our implants can result in massive savings to the healthcare system.”

______

About Paxeon Reconstruction

Paxeon Reconstruction builds best-in-class orthopaedic products, including derivative and emerging products. We collaborate with hospitals, health systems and physicians to create alignment and utilization of value-based solutions combined with efficiency models for today’s changing healthcare environment. Paxeon Reconstruction offer the world’s most comprehensive portfolio of orthopaedic products and services for joint reconstruction. Paxeon Reconstruction has a celebrated clinical history, and has evolved to meet the needs of the changing orthopaedics marketplace. The history that weaves the fabric of the Paxeon Reconstruction is one that is rich with innovation and demonstrates sustained leadership in an ever-changing landscape of patient and professional needs.

 


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September 25, 2017 OrthoSpineNews

BELLEAIR BLUFFS, Fla.Sept. 25, 2017 /PRNewswire/ — JointPoint, Inc., providers of non-invasive computer navigation, preoperative digital templating, case planning, and intra-operative feedback, is announcing that it has signed an exclusive agreement with DePuy Synthes to co-market its proprietary software platform. JointPoint™ integrates easily into the Direct Anterior Approach hip replacement technique.

“With over 1,000 cases completed over the last several months, surgeons are enjoying the benefits of JointPoint’s non-invasive hip navigation,” said Noah Wollowick, President and Co-Founder of JointPoint. “We are excited to solidify this co-marketing agreement with DePuy Synthes, a worldwide leader in orthopaedics, to gain better access to surgeons across the country that want to use our innovative technology.”

JointPoint’s intraoperative software streamlines fluoroscopic use while providing the surgeon significant data on cup position, leg length and offset. Additionally, JointPoint’s OneTrial™ technology incorporates implant specific data that has the potential to reduce trialing during surgery.

“I used to rely on multiple fluoroscopic images and trials to confirm a patient’s leg length and offset,” said Dr. Charles Decook, MD. “With the OneTrial™ technique from JointPoint, I am able to trial and shoot one fluoroscopic image, that is it. It tells me my offset and leg length and I am able to clearly pick the neck and head that works best for that patient.  It has not only made me more efficient but also more accurate. I wouldn’t even think of interpreting a fluoroscopic image now without JointPoint.”

Adding the JointPoint software to a surgeon’s protocol may help reduce leg length discrepancy and complications related to inaccurate cup placement and final implant selection – two of the most important considerations in hip replacement surgery – by providing pre-surgical digital templating and real-time, data-driven surgical decision making in the operating room.

JointPoint’s navigation system minimizes adoption challenges of the anterior approach surgical method for hip replacement by providing cup position, leg length and offset data for a surgeon using as few as 3 radiographic images.

“One of the major benefits of anterior approach hip replacement is the power of intraoperative fluoroscopy and its ability to improve implant positioning, something all surgeons strive for consistently,” said Andrew J. Cooper, M.D., JointPoint’s Chief Medical Officer and Co-Founder.  “JointPoint harnesses the potential of fluoroscopy and allows surgeon to meet this goal efficiently with minimal images.”

About JointPoint, Inc.

JointPoint, Inc. develops and markets software-driven medical technology for orthopaedics. The JointPoint™ software solution and OneTrial™ technology is a completely non-invasive navigation system for hip replacement surgery that provides intraoperative data and guides component selection while also optimizing efficiency within a surgical workflow. For more information, visit http://www.jointpoint.com

SOURCE JointPoint, Inc.


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September 19, 2017 OrthoSpineNews

September 18, 2017

CAMPBELL, Calif. & COLUMBUS, Ohio–(BUSINESS WIRE)–ZipLine Medical, Inc. today announced results from an economic study that showed that Zip Surgical Skin Closure reduced post-discharge costs for total knee arthroplasty (TKA) when compared to staples. Results were presented Friday at the Knee Society Members Meeting by Roger Emerson, MD, of the Texas Center for Joint Replacement, Plano, Texas.

“In the study, we saw that staples and the Zip are both fast to apply in the operating room, but in the post-discharge environment, staple-related issues, such as patient phone calls, emergency department visits, infection concerns and removal create extra work and extra cost in the long run,” said Dr. Emerson. “In addition, patients were apprehensive about staple removal and concerned when they saw redness around their staples, which in some cases triggered antibiotic prescriptions to avoid possible infection.”

The study encompassed 130 consecutive TKA patients, with half of subjects closed with staples and half closed with Zip Surgical Skin Closure. All surgeries were performed at the Texas Center for Joint Replacement by the same surgeon using the same approach and implant, and were closed by the same surgical physician’s assistant. Patients were followed from surgery to first clinic post-operative visit (day 21-28) for assessment.

The study findings showed that the Zip reduced all of the following measures when compared to staples:

  • 46 percent reduction in incision-related actual clinic costs
  • 60 percent reduction in incision-related phone calls
  • 60 percent reduction in incision-related clinic visits
  • 75 percent reduction in incision-related antibiotics prescribed

In addition, patients found the resulting scar from the Zip to be cosmetically more appealing, and the Zip device less painful to remove, than staples.

”In addition to actual emergency room, clinic and wound-related care costs, which can be considered ‘bundle-busters’ in a bundled care setting, there are opportunity costs to consider, where unreimbursed time responding to patient calls, concerns and staple removal results in less time spent on billable activities,” said Omar Alnachoukati, director of clinical research at the Texas Center for Joint Replacement. “In the study, we found a five times higher opportunity cost in the staple group.”

He continued, “Total joint arthroplasty is the largest expense for a single condition among Medicare beneficiaries, totaling $7 billion annually. With staples currently one of the primary methods currently used for TKA closure, this study suggests that replacing staples with the non-invasive Zip device has the potential to offer significant savings to the healthcare system.”

The Zip is a non-invasive and easy to use skin closure device that replaces sutures, staples, and glue for surgical incisions and lacerations. Clinical studies have demonstrated significant time savings, fewer wound complications and the ability to reduce post discharge healthcare costs. A patented force distribution design results in secure wound closure, excellent scar quality and high patient satisfaction. Unlike staples or sutures, there are no skin punctures with the Zip that can create pathways for bacteria. Benefits of the Zip have been demonstrated in clinical studies in orthopedic total joint arthroplasty, foot and ankle, pediatric cardiothoracic, electrophysiology, dermatology, and plastic and reconstructive surgery.

ABOUT ZIPLINE MEDICAL

ZipLine Medical is an innovator in cost-effective, non-invasive surgical skin closure devices that deliver high patient satisfaction and surgeon efficiency. Zip Surgical Skin Closure devices have been used in more than 100,000 cases and in over 30 countries worldwide. ZipLine Medical was founded by Amir Belson, M.D. and is headquartered in Campbell, CA. For more information, visit www.ziplinemedical.com.

Zip® Surgical Skin Closure devices are classified by the U.S. FDA as ‘Class I, 510(k) Exempt’ and have received the CE Mark and CFDA approval.

Contacts

Chronic Communications, Inc.
Michelle McAdam, 310.902.1274
michelle@chronic-comm.com


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September 14, 2017 OrthoSpineNews

QUEBEC CITYSept. 14, 2017 /PRNewswire/ — Bodycad has announced that the first personalized restoration procedures using its Unicompartmental Knee System in patients have been successfully performed.

Bodycad’s revolutionary system is designed to optimize personalized restoration of the patient’s unique anatomical features and kinematics. The system is based on proprietary 3D rendering of medical images of the patient’s anatomy, resulting in a better fit and the potential for improved clinical results and patient satisfaction.

“The personalized restoration enabled me to perform the procedure in an exact manner with minimal bone resection,” said Dr. Brian Hamlin, Co-Director of the Bone and Joint Center of Magee-Womens Hospital of University of PittsburghMedical Center, one of two orthopaedic surgeons to perform the procedure. “The reconstruction resulted in a well balanced knee with optimized tracking while avoiding overcorrection.”

Bodycad uses proprietary imaging algorithms to produce a precise 3D image of the patient’s knee. Its suite of Personalized Restoration Software enables a seamless integration of the image to implant process called the PREP (personalized restoration evaluation process). The efficient, rapid, and highly automated process is the only one of itskind in the world that is impeccably integrated between software and modern manufacturing such as 3D printing.

“I was involved throughout the production of the personalized restoration,” said Prof. Werner Siebert of Vitos Orthopedic Clinic Kassel and incoming President of the German Orthopaedic Society, who also performed the procedure. “I provided patient imaging, consulted with a Bodycad PREP Tech on the resulting rendering, and then reviewed and approved the final design. The result was an exceptional fit for the patient.”

“Everyone’s anatomy is unique and that’s why standardized implants have limitations,” says Jean Robichaud, President and Founder of Bodycad. “These recent procedures reinforce a growing body of evidence that demonstrates the benefit of personalized restorations.”

Earlier this year, the company received US and European clearance for its Unicompartmental Knee System and is working collaboratively with practitioners to offer this personalized approach to orthopaedics.

About Bodycad

Bodycad is a Quebec City-based developer and manufacturer of personalized orthopaedic restorations. They are the only company in the world to have a seamlessly integrated, purpose-built, CAD/CAM platform. Its proprietary approach offers patients a high level of conformity to their unique anatomy, with the potential for greater comfort, fit and durability that make the pursuit of orthopaedic perfection possible. Learn more at www.bodycad.com.

Contact

Andy McLeod
2035 rue du Haut-Bord
QuebecQuebec, Canada
G1N 4R7
(418) 527.1388
info@bodycad.com

 

SOURCE Bodycad


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September 8, 2017 OrthoSpineNews

ALBANY, New YorkSeptember 8, 2017 /PRNewswire/ —

According to the research report, the global market for Hip Reconstruction Devices stood at US$5.68 bn in 2016 and is expected to witness strong growth over the period from 2017 to 2022. Primary cemented hip replacement devices enjoy a much higher demand among all the products available in this market. With a rise to US$126.6 mn per annum in revenues, this segment is anticipated to retain its dominance over the forecast period. With an increasing patient pool, osteoarthritis and rheumatoid arthritis have emerged as the primary indication for the application of these devices. Researchers predict this trend to continue over the next few years. Hip reconstruction devices find significant application in hospitals, ambulatory surgical centers (ASCs), and orthopedic clinics.

View Full Report at http://www.transparencymarketresearch.com/hip-reconstruction-devices-market.html

“With the significant increase in the geriatric population base across the world, the prevalence of osteoporosis and rheumatoid arthritis is augmenting continuously, resulting in the soaring need for hip reconstruction surgeries, which, subsequently, is boosting the demand for hip reconstruction devices,” says a TMR analyst. The rising cases of hip injuries and the growing demand for minimally invasive procedures is also propelling the global hip reconstruction devices market remarkably.

Going forward, the technological advancements in hip reconstruction devices are likely to drive the growth in this market over the next few years. The upswing in the investments for research and development of highly advanced and minimally invasive hip reconstruction procedures and devices is also projected to have a positive impact on this market in the near future.

High Cost of Devices to Act as Restraint

The worldwide hip reconstruction devices market, although, looks thriving; however, the high cost of hip reconstruction procedures and devices may restrict the market from growing steadily in the coming years. The stringent regulations required for the approval for these devices will also create hindrances in the growth trajectory of this market over the next few years.

Nonetheless, the rising awareness pertaining to the benefits of hip construction procedures in treating patients and enabling them to perform daily activities and live a normal lifestyle is expected normalize the impact of these restraints in the years to come, states the study.

Request to View Sample Report – http://www.transparencymarketresearch.com/sample/sample.php?flag=S&rep_id=10307

Regionally, North America has emerged as the leading market for hip reconstruction devices across the world. Analysts at TMR anticipate this regional market for remain on the top over the forecast period on the grounds of the presence of established hip reconstruction device vendors in a large number. The increasing demand for minimally invasive surgeries is also projected to boost the North America market for hip reconstruction devices in the years to come, states the research report.

With a large pool of manufacturers, the global hip reconstruction devices market is demonstrating a high competitive and fragmented business landscape, finds a new research study by Transparency Market Research (TMR). Innovation and advancements in current offerings is the key trend among the leading players in this market, such as United Orthopedic, Exactech, Corin, Braun Melsungen, DePuy Synthes, Stryker and others. However, over the forthcoming years, a shift in their focus towards strategic alliances, in the form of mergers, acquisitions, and partnerships, can be observed, notes the research study.

Hip Reconstruction Devices Market Report IAvailable @ US$ 5795

About TMR

Transparency Market Research (TMR) is a global market intelligence company providing business information reports and services. The company’s exclusive blend of quantitative forecasting and trend analysis provides forward-looking insight for thousands of decision makers. TMR’s experienced team of analysts, researchers, and consultants use proprietary data sources and various tools and techniques to gather and analyze information.
Contact
Transparency Market Research
State Tower
90 State Street,
Suite 700,
Albany NY – 12207
United States
Tel: +1-518-618-1030
USA – Canada Toll Free: 866-552-3453
Email: sales@transparencymarketresearch.com

Website: http://www.transparencymarketresearch.com 
TMR Blog: http://www.theglobalhealthnews.com/

SOURCE Transparency Market Research


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September 6, 2017 OrthoSpineNews

September 06, 2017

CASTEL SAN PIETRO, Switzerland–(BUSINESS WIRE)–The number of surgeons adopting the anterior approach to hip replacement is on the rise, with an estimated 20 percent of hip surgeons now performing the procedure. Medacta International, the family-owned global leader in the design of innovative joint replacement and spine surgery products, is leading the charge in training and supporting surgeons transitioning to this muscle-sparing technique. Today, the company and the Medacta Orthopaedic Research and Education (M.O.R.E.) Institute announced the execution of the 250th M.O.R.E. AMIS® Learning Center, where surgeons from all over the world will come to learn Medacta’s Anterior Minimally Invasive Surgery (AMIS) technique, complete with a system of tools and educational resources designed to support surgeons practicing the anterior approach for hip replacement.

“The promotion of patient well-being through AMIS is a cornerstone of Medacta’s mission, as it exemplifies our belief that only with a strong focus on medical education can surgical innovation truly move the industry forward,” said Francesco Siccardi, Executive Vice President of Medacta International. “The patient-centric technique is also ideal for the outpatient or same-day surgery setting, providing more options for both surgeons and patients in today’s changing healthcare landscape.”

The AMIS technique, informed by decades of clinical experience, is a muscle-sparing approach to total hip replacement that is associated with potential positive patient outcomes like shorter hospitalization and rehabilitation time, as well as a faster return to daily activities.

Offered as part of the M.O.R.E. Institute, the M.O.R.E. AMIS Education Program is a comprehensive offering for surgeons seeking to become proficient in the technique, including ongoing medical education and dedicated implants and instruments. To date, more than 5,500 surgeons across 31 countries have received training through the program. At the end of 2016, that translated to more than 80,000 hours of proctoring and surgeon-to-surgeon mentoring. In the field, surgeons have performed more than 250,000 total hip replacements utilizing the AMIS platform so far.

“The anterior approach to hip replacement has also been gaining traction among patients who are attracted to the possibility of a faster recovery and return to their daily lives,” said Frédéric Laude, M.D., a pioneer of the technique from Paris, France. “There is a learning curve associated with the approach though, so both hands-on and technical support are crucial to success. The level of attention and support Medacta provides through its M.O.R.E. AMIS Education Program is unparalleled.”

The 250th M.O.R.E. AMIS Learning Center will be held September 15-16, 2017 in Chicago, IL, followed by a European installment September 25-26, 2017 in Basel, Switzerland. More information on the AMIS platform can be found at https://www.medacta.com/EN/amis.

About the M.O.R.E. AMIS Education Program

Education is the most crucial tool to drive clinical proficiency and innovation, as well as patient outcomes across the globe. To support positive outcomes in the operating room, Medacta created the AMIS Education Program, a comprehensive multistep training process within its M.O.R.E. Institute. The Program involves visiting a Reference Center to watch live surgery, attending a M.O.R.E. AMIS Learning Center, and ultimately performing surgery with support from an AMIS certified surgeon proctor. Throughout, product specialists and surgeons are available to provide mentorship and support. Approximately 85 percent of surgeons trained via the M.O.R.E. AMIS Education Program continue to use the approach once their training is complete.

About the M.O.R.E. Institute – “Where the surgeon is never alone”

Strongly aware of its role to provide continuing education as products and techniques evolve, Medacta International founded the Medacta Orthopaedic Research and Education (M.O.R.E.) Institute to highlight this commitment. Built on the ideal of sharing experience within the international medical community, the mission of the M.O.R.E. Institute is to provide ongoing support to Medacta partners worldwide as they strive to make an impact by learning about and adopting emerging technologies, surgical techniques and orthopaedic products. The Institute includes the M.O.R.E. AMIS Education Program for total hip arthroplasty, which has revolutionized the teaching of the anterior approach to hip replacement throughout the world, as well as platforms to impact the specialties of partial and total knee arthroplasty, total and reverse shoulder arthroplasty, sports medicine and spine surgery. The Institute relies on Medacta consultants and the healthcare provider community to create networking opportunities and hundreds of educational events, including courses, wet labs, scientific evenings, surgeon-to-surgeon visits, international symposia, guesting and hosting thousands of participants from all over the world. With a strong focus on young and promising surgeons, the M.O.R.E. Institute also supports fellowship programs worldwide.

About Medacta

Medacta® International is a world leading manufacturer of orthopedic implants, neurosurgical systems, and instrumentation. Medacta’s revolutionary approach and responsible innovation have resulted in standard of care breakthroughs in hip replacement with the AMIS®system and total knee replacement with MyKnee® patient matched technology. Over the last 10 years, Medacta has grown dramatically by taking a holistic approach and placing value on all aspects of the care experience from design to training to sustainability. Medacta is headquartered in Castel San Pietro, Switzerland, and operates in over 30 countries. To learn more about Medacta International, please visit www.medacta.com or follow @Medacta on Twitter.

Contacts

for Medacta International, Inc.
Jill Bongiorni, 516-729-2250
Jill@torchcomllc.com