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July 5, 2017 OrthoSpineNews

Smith & Nephew (LSE:SN, NYSE:SNN), the global medical technology business, and the University of Hull today announce a long-term collaboration driving research into pioneering approaches to advanced wound care.

The partnership will create one of the world’s largest Wound Care Research Clusters, combining world-leading academia and industry with the aim of developing scientific insights and innovative treatments for advanced wound care.

A five year framework has been established which sees a co-investment of around £3 million. Within this, eight multi-disciplinary PhD studentships have been created.

Dr David Richards, Pro-Vice Chancellor for Research and Enterprise at the University of Hull, said: “This partnership goes to further strengthen our links with industry at the same time as creating a global hub for pioneering new approaches in this field. By combining the considerable expertise we have at the University with those at Smith & Nephew, we will drive research which will help to position ourselves as global leaders in this field.”

Dr Matthew Hardman, Wound Healing Research Group Head, University of Hull, said: “I am delighted by the establishment of this exciting new multi-disciplinary wound care cluster. This venture brings together a team of experts from across the University and builds upon our existing links with a world-leader in advanced wound management. This exciting partnership will ultimately deliver significant patient benefits.”

The collaboration has been welcomed by new local MP Emma Hardy, who commented: “Britain is a global leader in medical technology innovation. Partnerships such as this between Smith & Nephew and University of Hullfurther strengthen our position at the forefront of global medical research and development. Creating one of the largest wound care clusters in the world is a huge vote of confidence in the UK as a whole and Hull in particular, as we build a ‘global Britain’ with pioneering medical technology at its heart.”

Supporting the collaboration is Smith & Nephew’s new state-of-the-art Research & Development (R&D) centre in Hull, UK, and the University of Hull’s £28-million new Health Campus, due to open in the summer. Smith & Nephew’s R&D hub for wound management technologies, which opened on 12 May, specialises in toxicology, chemistry and microbiology among other specialist fields. Smith & Nephew’s Hull site also manufactures some of the world’s most advanced wound care products, including pioneering products such as PICO, a unique single use negative pressure wound therapy system and ALLEVYN◊  Life advanced foam dressings.

The University of Hull’s new Health Campus is due to open in July this year. At its heart is the Allam Medical Building which will house the University’s new Institute for Clinical and Applied Health Research and includes specialist biomedical and clinical research facilities, as well as a mock hospital ward, operating theatre and intensive care nursing facilities.

Smith & Nephew will extend the use of its facilities to the Wound Care Cluster PhD students through dedicated workshops and providing industrial placement supervisors. University of Hull alumni make up around 25% of staff within wound research and development at Smith & Nephew in Hull, with many more across different roles within the company.

Stewart McKinlay, Vice President of Research & Innovation, Smith & Nephew, said “We are thrilled that the University of Hull shares our passion for the importance of advancing the science of wound care. Pioneering innovation is a strategic priority for Smith & Nephew. This partnership will combine the brightest minds with the finest R&D facilities available with the aim of better supporting healthcare professionals in the advanced treatment of wounds, which is an area of significant unmet medical need and a substantial cost to healthcare systems.

“There will be opportunities for students and employees to interact on a daily basis to share knowledge, best practice and support our ambitious R&D pipeline. Combine that with the scale of scientific specialities that is based here, then this partnership is a truly exciting prospect.”

 

Enquiries

Media
Charles Reynolds
Smith & Nephew

 

+44 (0) 1923 477314
Ben Atwell / Matthew Cole
FTI Strategic Consulting

 

+44 (0) 20 3727 1000
Investors
Ingeborg Oie
Smith & Nephew
+44 (0) 20 7401 7646
   


About Smith & Nephew

Smith & Nephew is a global medical technology business dedicated to helping healthcare professionals improve people’s lives. With leadership positions in Orthopaedic ReconstructionAdvanced Wound ManagementSports Medicine and Trauma & Extremities, Smith & Nephew has around 15,000 employees and a presence in more than 100 countries. Annual sales in 2016 were almost $4.7 billion. Smith & Nephew is a member of the FTSE100 (LSE:SN, NYSE:SNN).

For more information about Smith & Nephew, please visit our website www.smith-nephew.comfollow @SmithNephewplc on Twitter or visit SmithNephewplc on Facebook.com.

Forward-looking Statements

This document may contain forward-looking statements that may or may not prove accurate. For example, statements regarding expected revenue growth and trading margins, market trends and our product pipeline are forward-looking statements. Phrases such as “aim”, “plan”, “intend”, “anticipate”, “well-placed”, “believe”, “estimate”, “expect”, “target”, “consider” and similar expressions are generally intended to identify forward-looking statements. Forward-looking statements involve known and unknown risks, uncertainties and other important factors that could cause actual results to differ materially from what is expressed or implied by the statements. For Smith & Nephew, these factors include: economic and financial conditions in the markets we serve, especially those affecting health care providers, payers and customers; price levels for established and innovative medical devices; developments in medical technology; regulatory approvals, reimbursement decisions or other government actions; product defects or recalls or other problems with quality management systems or failure to comply with related regulations; litigation relating to patent or other claims; legal compliance risks and related investigative, remedial or enforcement actions; disruption to our supply chain or operations or those of our suppliers; competition for qualified personnel; strategic actions, including acquisitions and dispositions, our success in performing due diligence, valuing and integrating acquired businesses; disruption that may result from transactions or other changes we make in our business plans or organisation to adapt to market developments; and numerous other matters that affect us or our markets, including those of a political, economic, business, competitive or reputational nature. Please refer to the documents that Smith & Nephew has filed with the U.S. Securities and Exchange Commission under the U.S. Securities Exchange Act of 1934, as amended, including Smith & Nephew’s most recent annual report on Form 20-F, for a discussion of certain of these factors. Any forward-looking statement is based on information available to Smith & Nephew as of the date of the statement. All written or oral forward-looking statements attributable to Smith & Nephew are qualified by this caution. Smith & Nephew does not undertake any obligation to update or revise any forward-looking statement to reflect any change in circumstances or in Smith & Nephew’s expectations.

 

◊ Trademark of Smith & Nephew.  Certain marks registered US Patent and Trademark Office.

 


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July 5, 2017 OrthoSpineNews

July 03, 2017

HUNTLEY, Ill.–(BUSINESS WIRE)–Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders today announced the full commercial launch of key additions to the OSSEO-LOC™ spinal implant family.

ProLift® Expandable PLIF/TLIF Spacer System and TiBOW™ Expandable TLIF Spacer System join Life Spine’s OSSEO-LOC offering of titanium surface treated implants. OSSEO-LOC is a proprietary surface treatment that creates a unique osteophylic surface architecture for potential bone on-growth.1 The unique surface architecture promotes mineralization of implant, while negating potential challenges associated with surface treated implants.2 OSSEO-LOC surface treatment maintains native titanium grain structure and material, and has been designed to optimize intervertebral stability.1

Other key OSSEO-LOC implants include the static spinal spacer systems PLATEAU®-C (cervical spacer system), PLATEAU-Z Ti (TLIF spacer system), PRO-LINK® TI (stand-alone cervical spacer system), PLATEAU TI (straight and curved PLIF and TLIF spacer systems); SImpact™ lag and compression screws for sacroiliac fixation and stabilization.

Mariusz Knap, Vice President of Marketing noted, “We are excited to launch the key additions to the OSSEO-LOC family of spinal implants, as it deepens Life Spine’s commitment to provide surgeons with access to our highly differentiated, minimally invasive spinal products. Addressing a variety of pathologies, Life Spine’s procedural based solutions increase the value of care by delivering both the ability to correct spinal alignment and improved patient experiences and outcomes. This will be a driving force as we continue to expand Life Spine’s wide range of surgical solutions.”

About Life Spine

Life Spine is dedicated to improving the quality of life for spinal patients by increasing procedural efficiency and efficacy through innovative design, uncompromising quality standards, and the most technologically advanced manufacturing platforms. Life Spine, which is privately held, is based in Huntley, Illinois. For more information, please visit: http://www.lifespine.com.

Life Spine is a registered trademark.

1Feighan, J.E., Goldberg, V.M., Davy, D., Parr, J.A., Stevenson, S.
“The Influence of Surface Blasting on the Incorporation of Titanium-Alloy Implants in a Rabbit Intramedullary Model.” The Journal of Bone and Joint Surgery 77.9 (1995): 1380-96. Web.

2K.Kieswetter, Z. Schwartz, T. W. Hummert, D. L. Cochran, J. Simpson and B. D. Boyan
“Surface roughness modulates the local production of growth factors by osteoblast-like MG-62 cells” The Journal of Biomedical Materials Research (1996): Web.

Contacts

Life Spine
Mr. Omar Faruqi
Chief Financial Officer
ofaruqi@lifespine.com
847-884-6117


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June 30, 2017 OrthoSpineNews

OrthoSpace Ltd. (“OrthoSpace” or “the Company”) today announced the publication of positive data on the use of the InSpace™ subacromial spacer for the treatment of massive rotator cuff tears. The case series of 39 shoulders (37 patients) was published in Arthroscopy and demonstrated improved function and reduced pain in patients treated with the InSpace System.

“Patients who fail conservative therapy for massive rotator cuff repair have historically had few options for further treatment of this debilitating, painful condition,” said Julien Deranlot, M.D., principal investigator of the study and an orthopedic surgeon at Clinique Drouot in Paris, France. “The InSpace provides a safe and reliable surgical alternative that can improve shoulder pain and function, allowing patients to have a better quality of life post-operatively.”

The InSpace System consists of a biodegradable balloon spacer deployed in the subacromial space between the acromion and the humeral head, allowing smooth gliding and frictionless movement between the two bones and emulating the function of the original bursa. It is usually placed arthroscopically in a procedure that requires only 10 minutes to perform.

This study assessed clinical, functional and radiographic outcomes for all patients with symptomatic massive irreparable rotator cuff tears who were treated with the InSpace at the Clinique Drouot between January 2011 and December 2014. Patients included in this study had a minimum of one year and up to three years of follow-up at the time of analysis.

The investigators reported the following results:

  • Range of motion was significantly increased for all patients in anterior elevation, abduction and external rotation.
  • The mean Constant score, which measures pain, activity level and function, improved from 40 (±14.6) (45 [±15.2] when adjusted for age and gender) at baseline to 59 (±13.7) at one year, and up to 64 (±13.6) (adjusted = 76 [±17.1]) (P < 0.0001) at last follow-up. Notably, there was a significant improvement between the one-year follow-up and three-year follow-up regarding the adjusted Constant score (P=0.02).
  • At last follow-up, adjusted Constant score was excellent (greater than 100 points) for three shoulders (9%), good (86-99 points) for eight (23%), fair (65-85 points) for sixteen (45%), and poor (fewer than 65 points) for eight shoulders (23%).
  • Among the radiographic outcomes, when assessing for Hamada score (a measure of osteoarthritis), four shoulders progressed by one radiographic stage (15%), and two shoulders progressed by three stages (4%). 32 shoulders had no progression during follow-up.

“We continue to be encouraged by the compelling clinical improvements we see in patients treated with the InSpace System, which are in line with the strong results demonstrated in previous studies,” OrthoSpace CEO Itay Barnea commented. “The system offers a safe, minimally invasive option that can be effectively used to relieve pain and improve shoulder function for patients, especially in elderly patients with chronic pain and disability, poor tissue quality or other health issues, who may not have alternative treatment options.”

The InSpace System is CE Marked in Europe and Israel and is investigational in the U.S. and Canada, where it is currently being evaluated in a prospective, single-blinded, multi-center, randomized, controlled study that will enroll up to 184 patients.

About OrthoSpace Ltd.
OrthoSpace is a privately held medical device company located in Caesarea, Israel. The Company’s product, InSpace, is an orthopedic biodegradable balloon system that is simple, safe and a minimally invasive method that addresses unmet clinical needs in rotator cuff repair. InSpace is CE Marked and commercialized in Europe and Israel and has been granted an Investigational Device Exemption (IDE) to initiate a pivotal human clinical study of the InSpace System in the United States.


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June 30, 2017 OrthoSpineNews

Posted 29 June 2017 – By Michael Mezher

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) on Thursday issued an alert to healthcare professionals with updated recommendations for long-term follow-up for patients with metal-on-metal hip replacements.

Safety and durability concerns about metal-on-metal hip replacements, along with a scandal involving faulty breast implants, were a driving factor in the EU’s decision to overhaul its medical device and in vitro diagnostics regulations.

Previously, MHRA’s recommendations focused on larger metal-on-metal hip replacements (≥36mm) and certain implants made by Johnson & Johnson subsidiary DePuy Synthes, which were thought to be riskier than other types of metal-on-metal hips.

In August 2010, DePuy recalled two models of its ASR hip replacement systems, and in 2013 the UK’s National Health Service (NHS) stopped performing most metal-on-metal hip replacements, citing high failure rates. However, tens of thousands of patients in the UK still have the devices implanted.

 

READ THE REST HERE


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June 30, 2017 OrthoSpineNews

WARSAW, Ind., June 30, 2017 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH) today announced its second quarter sales and earnings conference call will be broadcast live over the Internet on Thursday, July 27, 2017, at 8 a.m. Eastern Time.  A news release detailing the quarterly results will be made available at 7:30 a.m. Eastern Time the morning of the conference call.

The live audio webcast can be accessed via Zimmer Biomet’s Investor Relations website at http://investor.zimmerbiomet.com. It will be archived for replay following the conference call.

Individuals in the U.S. and Canada who wish to dial into the conference call may do so by dialing (888) 312-9837 and entering conference ID 7278985.  For a complete listing of international toll-free and local numbers, please visit http://investor.zimmerbiomet.com.  A digital recording will be available 24 hours after the completion of the conference call, from July 28, 2017 to August 26, 2017.  To access the recording, U.S. callers should dial (888) 203-1112 and international callers should dial +1 (719) 457-0820, and enter the Access Code ID 7278985.

About the Company

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.

ZBH – Fin

SOURCE Zimmer Biomet Holdings, Inc.

Related Links

http://www.zimmer.com


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June 30, 2017 OrthoSpineNews

BY

BoneSupport said last week it closed its initial public offering, raising a total of approximately $57.1 million (SEK 500 million), not including an over-allotment option.

The Swedish company, which is developing the Cerament G injectable antibiotic-eluting bone graft substitute, said it floated approximately 17.2 million new shares at $3.40 per share (SEK 29) in the round, raising approximately $57.1 million before issue costs and $54 million (SEK 461 million) after issue costs.

Bonesupport also issued an over-allotment option for 2.6 million shares and an additional $8.7 million (SEK 75 million), bringing the total number of shares offered in the round to 48.8 million, according to a press release.

 

READ THE REST HERE


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June 30, 2017 OrthoSpineNews

ATLANTA, June 29, 2017 /PRNewswire/ — Meditech Spine, LLC, announced today it has received 510(k) clearance for its CURE Lumbar Plating (LP) System from the US Food and Drug Administration (FDA). The CURE LP allows surgeons to utilize the lumbar plating system along with Meditech’s innovative lumbar Talos® fusion devices, which are manufactured with PEEK-OPTIMA™ HA Enhanced polymer offered by Invibio Biomaterial Solutions. These devices are essential in the market, as an estimated 25 percent of thoraco-lumbar interbody fusions are performed via the anterior and lateral approaches.

The CURE LP is:

  • A low profile titanium plate that incorporates a proprietary, one-step locking mechanism to prevent bone screws anchored on the spine from loosening and backing out.
  • Designed with a large graft window for viewing the interbody space.
  • Pre-lordosed for lumbar sacral applications.
  • Available for both anterior and lateral procedures as four-hole or two-hole plates.

“As the anterior and lateral surgical approaches continue to grow, especially as they relate to global sagittal balance and alignment of the spine, we are pleased to receive this clearance so quickly after the clearance for our ALIF and LLIF Talos® HA Peek spacers earlier this month,” says Eric Flickinger, co-founder of Meditech Spine. “This accomplishment is really a testament to our team for their focused efforts in achieving two major milestones this year, and we are privileged to add value to our implant solutions for surgeons and their patients.”

The CURE LP and Talos®-A (HA) Lumbar IBF device will be combined in one tray with streamlined instruments to make it easier for hospital and surgery centers to process the system. Both systems will be provided sterile and pre-packaged to reduce implant related infections and help with implant tracking.

Meditech began its partnership with CURE International, an organization that serves children with physical disabilities in underserved areas of the world, during the development of its CURE Anterior Cervical Plate (ACP), introduced last year. “We are excited to continue building upon our relationship with CURE International and inspired to see how they work tirelessly around the world, bringing healing and hope to those who are less fortunate,” says Flickinger. A portion of proceeds from the sale of every CURE LP plate will help CURE International treat patients in underserved areas who are in need of surgical care.

For more information visit Meditech Spine.

ABOUT MEDITECH SPINE, LLC

Meditech Spine, LLC, is a spinal device company developing innovative instrumentation for treating complex spinal issues. It partners with leaders in the industry to design, develop, and distribute implant devices that make a positive difference in the market. Meditech’s pursuit of novel and innovative technologies drives its design and development team. As Meditech builds on its IP platform, it seeks strategic partnerships and applications to provide surgeons and patients with the best available technologies.

CONTACT

Meditech Spine, LLC
(678) 974-5287
support@meditechspine.com

Caption & Copyright:

Talos® and Meditech logos are registered trademarks of Meditech Spine, LLC. All rights reserved.

INVIBIO™, PEEK-OPTIMA™, INVIBIO BIOMATERIAL SOLUTIONS™ are registered trademarks of Invibio, Ltd. All rights reserved.

 

SOURCE Meditech Spine, LLC

Related Links

http://www.meditechspine.com/


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June 30, 2017 OrthoSpineNews

Who should be named Startup of the Year from the West [Pacific – Southern California] region? You can share your opinion by voting for your favorite startup in our Reader’s Choice Poll below. Reader’s Choice Poll voting will help guide the selection of the top 100 startup semifinalists who will compete for cash, prizes and more, at the Innovate! and Celebrate conference in San Francisco on October 9th – 11th, 2017. The deadline to vote is July 12th.

There’s a “Click to Vote” link next to each startup below, vote for the startup you like the best located in the West [Pacific – Southern California] region:

Airspace Technologies (Carlsbad, CA) [Click to Vote]
Airspace Technologies offers end-to-end logistics solutions: we take a modern approach to time critical shipments by enabling technology.

Bezelhub (Santa Monica, CA) [Click to Vote]
Bezelhub is jewelry in your pocket. Just tap a button and a luxury watch is delivered right to you, giving you the access you need, anywhere.

Blue (Riverside, CA) [Click to Vote]
Blue is a mobile application that introduces people using bluetooth low energy without the touch of a button.

Bottlerocket (Santa Monica, CA) [Click to Vote]
BottleRocket is the first on-demand service that rewards users for recycling.

Decorator (Santa Monica, CA) [Click to Vote]
Decorator is crowdsourcing interior design. Think The Sims for real-life homes where other people redesign your room with new paint & furniture.

LineStar by Fantasy Sports Co. (San Diego, CA) [Click to Vote]
Fantasy Just Got Fun Again as LineStar is the #1 Companion for DraftKings, FanDuel, and Yahoo Daily Fantasy!

GoShare (San Diego, CA) [Click to Vote]
GoShare connects truck and van owners with people and business who need help moving, hauling and delivering large items on demand.

Lemonlight (Marina del Rey, CA) [Click to Vote]
Lemonlight creates high-quality affordable video content at scale. In 3 years, the company has produced 4000+ videos for brands nationwide.

LuxeRoom4Day (Beverly Hills, CA) [Click to Vote]
LuxeRoom4Day is a simple, fast, and secure way to book a 5-star luxury hotel day rooms, with prices up to 70 percent cheaper than the night rates.

Markett (Venice, CA) [Click to Vote]
Markett is a performance based platform that systematizes word of mouth marketing by providing ambassadors with all the tools they need to acquire new customers for their favorite brands.

Nutra.io (Playa Vista, CA) [Click to Vote]
Nutra.io is an end-to-end solution to decoding your genetic data into actions to help you eat right and supplement your body based on your genome and track your results.

Oska Wellness (Carlsbad, CA) [Click to Vote]
Oska Wellness is a new health-tech, wearable pain relief device that can help areas of the body prone to injury and degeneration.

Raken (Carlsbad, CA) [Click to Vote]
Raken’s software is a shot of adrenaline for a construction industry still stuck in the paper and pencil era.

Renly (Manhattan Beach, CA) [Click to Vote]
A marketplace for renters and sub-renters.

RepWatch (Westlake Village, CA) [Click to Vote]
RepWatch promotes efficient recovery for physical therapy patients by providing a system that encourages and motivates patients to stay on track.

SPARE. (Santa Monica, CA) [Click to Vote]
SPARE. is a community-based cash network allowing cash-back without a purchase. We empower merchants to dispense cash directly from their cash registers and consumers order cash directly from their mobile devices.

SwiftChange (San Diego, CA) [Click to Vote]
SwiftChange lets you receive change on your phone after a cash payment so you can capture the value of change without the hassle of coins!

Tampon Tribe (Santa Monica, CA) [Click to Vote]
Tampon Tribe is a movement that offers affordable access to organic feminine hygiene via online subscription for $8 a month and deliver to your home.

Trulo (Manhattan Beach, CA) [Click to Vote]
Trulo is the home for your best kept secrets of your locals-only spots in your city that you share with your hand-selected travel tribe.

Youngry (Newport Beach, CA) [Click to Vote]
Youngry provides early stage entrepreneurs “Young In Spirit, Hungry In Ambition” the best mentor driven content on the planet.

Thank you to our Startup of the Year sponsors and partners


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June 29, 2017 OrthoSpineNews

RAYNHAM, Mass., June 29, 2017 /PRNewswire/ — Today DePuy Synthes* announces the U.S. launch of the VIPER® and EXPEDIUM® Fenestrated Screw Systems. When used in conjunction with CONFIDENCETM High Viscosity Spinal Cement, the screws are intended to restore the integrity of the spinal column in patients with advanced stage spinal tumors. The fenestrated screw systems provide stabilization and palliative treatment for patients who may be suffering from spinal cord compression as a result of advanced stage tumors.

Surgical treatment for patients with advanced stage spinal disease can be challenging with traditional pedicle screw systems, but using fenestrated screws with spinal cement can provide immediate screw fixation while stabilizing the spine. The VIPER and EXPEDIUM Fenestrated Screws are designed with a hollow shaft, or cannulation. This design along with fenestrations above the screw tip enable controlled delivery of CONFIDENCE High Viscosity Spinal Cement into the vertebra to provide immediate screw fixation.

“The ability to inject cement via fenestrated screws is a true game-changer in the field of spinal oncology,” said Daniel Sciubba**, M.D., Director, Spine Tumor and Spine Deformity Surgery, Johns Hopkins Hospital. “The systems are reliable and easy-to-use and can seamlessly be incorporated into open and minimally invasive approaches. The cement working characteristics, delivery system and ability to use standard hardware and tools make the systems extremely efficient.”

The VIPER and EXPEDIUM Fenestrated Screw Systems may be used in open or percutaneous spinal fusion surgery. The use of VIPER Fenestrated Screws combined with spinal cement can be used in minimally invasive surgery (MIS), a type of surgery that is associated with a reduction in operating room time, blood loss and lower infection rates. The VIPER Fenestrated Screws are compatible with the instrumentation of the VIPER and EXPEDIUM 5.5 Spine Systems, and the EXPEDIUM Fenestrated Screws are compatible with the instrumentation of the EXPEDIUM VERSE® Spinal System. Both fenestrated screw systems are now available nationwide.

Indications for Use

When used in conjunction with CONFIDENCETM High Viscosity Spinal Cement, the VIPER® and EXPEDIUM® Fenestrated Screw Systems are intended to restore the integrity of the spinal column even in the absence of fusion for a limited time period in patients with advanced stage tumors involving the thoracic and lumbar spine in whom life expectancy is of insufficient duration to permit achievement of fusion. The VIPER® and EXPEDIUM® Fenestrated Screw Systems augmented with the CONFIDENCETM High Viscosity Spinal Cement are for use at spinal levels where the structural integrity of the spine is not severely compromised.

About DePuy Synthes Companies
DePuy Synthes Companies, part of the Johnson & Johnson Medical Devices Companies***, provides one of the most comprehensive orthopaedics portfolios in the world. DePuy Synthes Companies solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit www.depuysynthes.com.

*DePuy Synthes represents the products and services of DePuy Synthes, Inc. and its affiliates. Medos International SARL is the legal manufacturer of the VIPER® and EXPEDIUM® Fenestrated Screw Systems.
**Consultant to DePuy Synthes Spine
***The Johnson & Johnson Medical Devices Companies comprise the surgery, orthopaedics, and cardiovascular businesses within Johnson & Johnson’s Medical Devices segment.

©DePuy Synthes 2017. All rights reserved.
DSUS/SPN/0617/1615(1)

 

SOURCE DePuy Synthes

Related Links

http://www.depuysynthes.com


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June 29, 2017 OrthoSpineNews
Jody Stallings, Industrial Creations – 06.28.17
3D printing is becoming an important tool in nearly every industry today, but one area where it is really making an impact is in the medical field.
Doctors and surgeons can use 3D printed organ or bone models to explain to patients or students the details of a surgery or to practice the surgery itself. Other surgeons are actually designing their own prototypes of new surgical tools or bone replacement options.
The challenge, historically, is that 3D printing can be expensive and difficult to complete.
As a mechanical engineer, I began my career in automation design and robotics, but moved into the medical industry in 1990 when I was hired by an orthopedic knee replacement company. They asked me to utilize my experience to automate the process for finishing knee implants. It was a three-year project and the result was a new process that produced a knee implant in minutes instead of hours.
During that process, I saw the opportunity that surgeons have to develop new techniques and tools to enhance surgical procedures, but they lacked the resources to turn their ideas into a reality. Now, in my spare time I work with the doctors and surgeons to brainstorm a design based on their idea and 3D print it so that they can pitch to companies for production.
So, how does it all work?
An orthopedic surgeon comes up with an idea and it is then modeled using computer-aided design (CAD) software. The design is then printed using a desktop ABS 3D printer to fabricate the first conceptual models and get the surgeon to a point where they are happy with the design and are confident the part will be functional.
Up to this point, it’s fairly easy to manage time and expenses. However, when it comes time for a real functional prototype, that means working with metal and that’s when the costs start to increase. As the surgeons are often doing this on their own time and paying for it from their own pocket, it’s important that costs are managed.