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Current Issues in Spine

February 2-4, 2017

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June 22, 2017 OrthoSpineNews

From professional golfer Tiger Woods’ multiple spine surgeries dating back to 2014, to Golden State Warriors head coach Steve Kerr’s failed back surgery in 2015 and its resulting complications, a very bright public spotlight has been placed on the efficacy of spine surgery. The understandable question on many an “average Joe’s” mind is: If it didn’t work for them, how can it possibly work for me? The answer to that question requires a much deeper exploration of the intent of spine surgery and the many considerations required of both the surgeon performing it and the patient undergoing it.

First, it’s important to point out that success stories abound for many people who have experienced enough spine trouble to lead them down the path of exploring surgery to fix it. Some credit their new pain-free life to their spine surgeon after a successful surgery because they believe they’ve been given a second chance at a fully functional life. These quality of life transformations are awe-inspiring, and as a spine surgeon, these stories of success are my greatest victories and deepest sources of inspiration.

Though I have made spine surgery my career and have utmost confidence that a successful operation can change someone’s life for the better, the fact remains that sometimes spine surgery does fail. Now, you may be thinking, why would a spine surgeon tell me this? The answer is simple: honesty. The truth is, there are many reasons why a spine surgery may or may not work, and it’s my job to ensure that every one of my patients and the public, who may be considering surgery, thoroughly understands the benefits and risks before deciding on any type of spine treatment.

 

READ THE REST HERE


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June 21, 2017 OrthoSpineNews

MINNETONKA, Minn., June 21, 2017 /PRNewswire/ — Zyga Technology, Inc., a medical device company focused on the design, development and commercialization of minimally invasive devices to treat underserved conditions of the lumbar spine, today announced the issuance of a new US Patent representing continued advancement of the SImmetry Sacroiliac Joint Fusion System.

US patent number 9,662,124 relates to the design of the company’s proprietary SImmetry Decorticator®. This surgical instrument enables surgeons to prepare the sacroiliac (SI) joint for fusion by creating bleeding bone and space for autologous bone graft. This is accomplished through a minimally-invasive, lateral approach that avoids disruption of supporting ligaments around the SI joint.

Earlier this year the Company released results of a 19-patient, prospective, multi-center study of Minimally Invasive Sacroiliac Joint Fusion Surgery with Decortication. At 24 months post-op, 94 percent of patients had evidence of bridging bone across the SI joint, with 83 percent categorized as solid fusion. Of patients with solid fusion, 88 percent of the joints were fused within the area of decortication, demonstrating the importance of this step in achieving fusion. In addition to fusion, the study demonstrated a 73 percent reduction in average pain. Based on these data, the Company is currently sponsoring the EVoluSIon Study, a prospective, 40-site, 250-patient trial to evaluate long-term fusion and pain reduction in patients receiving SImmetry® Sacroiliac Joint Fusion.

“Zyga remains committed to advancing true fusion technology and the field of SI joint fusion,” said Jim Bullock, president and CEO of Zyga. “Zyga now has seven issued patents related to preparing the SI joint to establish a true biologic fusion.  The expansion of our intellectual property and ongoing support of clinical trials such as the EVoluSIon study further demonstrate Zyga’s leadership in innovation for minimally-invasive spine surgery.”

The Centers for Disease Control and Prevention lists back problems as the second most common cause of disability in U.S. adultsi. It has been reported that approximately 20 percent of all chronic LBP derives from the sacroiliac jointii.

About Zyga Technology, Inc.

Zyga Technology, Inc. is dedicated to the research, development and commercialization of solutions that provide empirical clinical and economic value in the treatment of underserved conditions of the spine. The company is marketing the SImmetry® Sacroiliac Joint Fusion System, a minimally invasive procedure intended for conditions including sacroiliac joint disruptions and degenerative sacroiliitis, and is conducting a U.S. multicenter clinical study of the Glyder Facet Restoration Device, a non-fusion, minimally invasive technology intended to provide relief from lumbar facet pain. For more information, visit zyga.com.

i Centers for Disease Control and Prevention. Prevalence of disabilities and associated health conditions among adults—United States, 1999. JAMA. 2001; 285(12):1571-1572.
ii Cohen SP et al. Sacroiliac Joint Pain: A Comprehensive Review of Epidemiology, Diagnosis and Treatment. Expert Rev Neurother. 2013; 13(1):99-116

CONTACT:
Erin Morrison
Tel 952 698 9956
emorrison@zyga.com

SOURCE Zyga Technology, Inc.

Related Links

http://www.zyga.com


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June 21, 2017 OrthoSpineNews

June 21, 2017

PARIS & SAN FRANCISCO–(BUSINESS WIRE)–Regulatory News:

SpineGuard (Paris:ALSGD) (FR0011464452 – ALSGD), an innovative company that develops and markets disposable medical devices designed to make spine surgery safer, announced today an exclusive distribution agreement with XinRong Medical Group for PediGuard® in China, Hong Kong and Macau.

China’s spine market has become the world’s second-largest market after the USA and is expected to be worth over $1 billion by 20191, driven by an aging population, increasing disease prevalence and treatment rates, along with growing affordability.

We are excited about this agreement and believe that XinRong Medical Group has all of the right attributes to successfully introduce PediGuard® in China, a market with great commercial potential. The number of spine fusions continues to grow rapidly across the country creating a substantial need for an easy-to-use smart device to secure the placement of pedicle screws consistently. Since its clearance by CFDA, numerous Chinese orthopedists and neurosurgeons have expressed a strong interest for our DSG™ technology. We now very much look forward to seeing them adopt it in their spine surgery practice,” said Pierre Jérôme, CEO and co-founder of SpineGuard.

“XR Medical is delighted to partner with SpineGuard, the company that owns PediGuard® and DSG™ technology. PediGuard® is the only one of its kind, and XinRong Medical is very excited to introduce one of the most advanced surgical solutions globally to the China market. SpineGuard’s cutting-edge technology allows surgical staff and patients to significantly reduce exposure to surgical radiation in the operating room while helping surgeons achieve more precise spinal implantation in real time. Ease of use, cost effectiveness, accuracy, and safety are the benefits that we want to bring to surgeons in China, through which we will continue to realize our vision of putting patients first,” added Christine Zhang, XinRong Medical Group’s CEO.

Next financial press release: 2017 Half-year revenue: July 6, 2017

About SpineGuard®
Founded in 2009 in France and the USA, by Pierre Jérôme and Stéphane Bette, SpineGuard’s mission is to make spine surgery safer by bringing real-time digital technology into the operating room. Its primary objective is to establish its proprietary DSG™ (Dynamic Surgical Guidance) technology as the global standard of surgical care, starting with safer screw placement in spine surgery and then in other surgeries. PediGuard®, the first device designed using DSG, was co-invented by Maurice Bourlion, Ph.D., Ciaran Bolger, M.D., Ph.D., and Alain Vanquaethem, Biomedical Engineer. It is the world’s first and only handheld device capable of alerting surgeons to potential pedicular or vertebral breaches. Over 50,000 surgical procedures have been performed worldwide with DSG™ enabled devices. Numerous studies published in peer-reviewed medical and scientific journals have demonstrated the multiple benefits that PediGuard® delivers to patients, surgical staff and hospitals. SpineGuard is expanding the scope of its DSG™ platform through strategic partnerships with innovative medical device companies and the development of smart instruments and implants. SpineGuard has offices in San Francisco and Paris. For further information, visit www.spineguard.com.

About XinRong Medical Group
XinRong Medical Group, a leader in medical technology, is dedicated to increasing patient affordability and providing the most advanced solutions for surgeons such that they can deliver the best patient care. XinRong Medical offers innovative solutions in orthopedic surgery, neurosurgery, reconstructive surgery, and minimally invasive therapy. Established in 2000 in Jiangsu Province, China, XinRong Medical was one of the first companies in China cleared by CFDA to manufacture Orthopedic Implants. In 2014, the Company received a strategic investment from The Blackstone Group (NYSE: BX). For additional information about XinRong Medical, please refer to our website www.XRBest.Com, or contact us directly at +86-512-58100828 or info@xrmed.com.

Disclaimer
The SpineGuard securities may not be offered or sold in the United States as they have not been and will not be registered under the Securities Act or any United States state securities laws, and SpineGuard does not intend to make a public offer of its securities in the United States. This is an announcement and not a prospectus, and the information contained herein does and shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of the securities referred to herein in the United States in which such offer, solicitation or sale would be unlawful prior to registration or exemption from registration.

1 according to IData Research

Contacts

SpineGuard
Manuel Lanfossi, +33 (0)1 45 18 45 19
Chief Financial Officer
m.lanfossi@spineguard.com
or
Europe / NewCap
Investor Relations & Financial Communication
Florent Alba / Pierre Laurent, +33 (0)1 44 71 94 94
spineguard@newcap.fr
or
US
Ronald Trahan Associates Inc.
Ronald Trahan, APR, +1-508-359-4005, x108


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June 21, 2017 OrthoSpineNews

Emerging Implant Technologies GmbH (EIT), a German medical device manufacturer exclusively focused on creating innovative technologies for spinal application by utilizing additive manufacturing, announces major milestones in preparation of its expected 510(k) approval later this year. EIT Cellular Titanium® is a porous titanium structure that has been designed according to scientific insights on ideal pore shape and size to optimize bone ingrowth. Due to the availability of Selective Laser Melting (SLM) technology and post-processing methods, it has been possible to create a highly porous, osteo-influential titanium scaffold for osseointegration. This EIT Cellular Titanium® structure has been applied in the complete ALIF, TLIF, PLIF and Cervical implant line, and clinical case studies and retrieval analysis demonstrate extensive bone ingrowth throughout the total implants in the cervical and lumbar spine in a short time frame.

To prepare for the launch of its innovative cellular titanium interbody devices, EIT has completed 3 major milestones. First, EIT has created a subsidiary and located its US Headquarters in Atlanta, GA. This move demonstrates its commitment to the US marketplace.

The second step EIT has made towards commercialization is by engaging GlobalMed Logistix (GMLx) to support its US distributors and surgeons by providing Warehousing, Supply Chain, Inventory Management and Customer Service. GlobalMed Logistix is a third-party logistics (3PL) company born from a rich 35-year distribution and warehousing history that will help coordinate and efficiently manage EIT’s logistics in the US.

Lastly, to help with Market Knowledge and Access, EIT has engaged Ortho Sales Partners (OSP). The primary areas of service that will be provided by OSP to EIT is Surgeon Access, Distributor Recruitment and Onboarding, Hospital Approvals and National Contracts through Group Purchasing Organizations (GPO) an Integrated Delivery Networks (IDN). Armed with the experience of the top industry talent, OSP leverages its team to help its clients shorten the cycle from launch to revenue.

Guntmar Eisen, Co-Founder and CEO for EIT says “We are very pleased to be partnered with these organizations in advance of our anticipated FDA Approval to help us deliver these innovative implants to US surgeons and patients. Our implants offer a combination of solid and cellular implant architecture to facilitate the rebuilding of natural cortical and cancellous bone structures while maintaining excellent imaging characteristics and we are eager to get started with our commercialization process.”

______

About EIT

EIT is the first medical device manufacturer to exclusively focus on spinal implants that are  designed according to latest published science on optimal bone ingrowth in porous titanium scaffolds and produced with additive manufacturing methods.

The EIT implants are made of EIT Cellular Titanium®, that addresses the clinical shortcomings of the current cage designs and materials (non-fusion, biocompatibility, subsidence, migration and imaging distortion), thereby obtaining very promising fusion results and improved clinical outcome due to the qualities of the porous 3-D printing of titanium. The highly porous titanium scaffold ensures extensive bone ingrowth as a result of its specific design and elasticity close to the cancellous bone. The limited amount of titanium material in the EIT implant ensures uncompromised imaging on X-ray and MRI and enabling excellent follow up on defining bone ingrowth and fusion with CT.

A complete portfolio of Smart Spinal Implants™ based on EIT Cellular Titanium® is available for the cervical and lumbar spine, with an extensive choice in footprint sizes, heights and lordosis angles to address the various anatomical requirements.  Over 10.000 cases have been performed in over 15 markets globally since 2014.

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June 20, 2017 OrthoSpineNews

LEESBURG, Va., June 20, 2017 (GLOBE NEWSWIRE) — K2M Group Holdings, Inc. (NASDAQ:KTWO) (the “Company” or “K2M”), a global leader of complex spine and minimally invasive solutions focused on achieving three-dimensional Total Body Balance, today announced the introduction of the SAHARA AL Expandable Stabilization System, the Company’s first expandable offering within its interbody portfolio. SAHARA AL is the only lordotic expandable interbody device with integrated screw fixation on the market to help achieve spinal balance.

The SAHARA AL Expandable Stabilization System represents a technological advancement over static interbody options, allowing for in-situ lordotic adjustment to match a patient’s sagittal profile through one fusion device. SAHARA AL is a zero-profile device with multi-screw fixation, designed to provide stability to the anterior column, while featuring a comprehensive range of lordotic adjustments of up to 26 degrees. It is indicated as a standalone device for lordotic angles of 15 degrees or less. SAHARA AL is manufactured from commercially pure grade II titanium, titanium alloy, and cobalt chrome.

“The anterior-lumbar interbody fusion (ALIF) approach allows for greater segmental lordosis correction and implant fixation than other alternative interbody approaches,” said Christopher Good, MD, FACS an orthopedic surgeon and Director of Scoliosis and Spinal Deformity at The Virginia Spine Institute in Reston, Virginia. “With variable in-situ lordotic adjustment, the SAHARA AL implant helps achieve sagittal balance and segmental reduction not generally attainable by ALIF cages with fixed lordotic angles.”

SAHARA AL features K2M’s innovative tifix® Locking Technology, which offers benefits such as allowing repeated screw adjustment up to three times, without compromising the locking feature. In addition, SAHARA AL features a comprehensive offering of footprints and heights to best fit patient anatomy.

“The introduction of the SAHARA AL Expandable Stabilization System marks a significant addition to our interbody portfolio as our first expandable offering in this category and the only device of its kind on the market today,” said Eric Major, President and CEO of K2M. “This latest milestone—coupled with the launch of our comprehensive, next-generation Balance ACS platform earlier this year—further reinforces our commitment to developing differentiated technologies with the goal of facilitating Total Body Balance.”

Balance ACS (BACS) is a comprehensive platform applying three-dimensional solutions across the entire clinical care continuum to help drive quality outcomes in spine patients. BACS provides solutions focused on achieving balance of the spine by addressing each anatomical vertebral segment with a 360-degree approach to the axial, coronal, and sagittal planes, emphasizing Total Body Balance as an important component of surgical success.

For more information on the SAHARA AL Expandable Stabilization System and K2M’s complete product portfolio, visit www.K2M.com. For more information about Balance ACS, visit www.BACS.com.

About K2M

K2M Group Holdings, Inc. is a global leader of complex spine and minimally invasive solutions focused on achieving three-dimensional Total Body Balance. Since its inception, K2M has designed, developed, and commercialized innovative complex spine and minimally invasive spine technologies and techniques used by spine surgeons to treat some of the most complicated spinal pathologies. K2M has leveraged these core competencies into Balance ACS, a platform of products, services, and research to help surgeons achieve three-dimensional spinal balance across the axial, coronal, and sagittal planes, with the goal of supporting the full continuum of care to facilitate quality patient outcomes. The Balance ACS platform, in combination with the Company’s technologies, techniques, and leadership in the 3D-printing of spinal devices, enable K2M to compete favorably in the global spinal surgery market. For more information, visit www.K2M.com and connect with us on Facebook, Twitter, Instagram, LinkedIn, and YouTube.

Forward-Looking Statements

This press release contains forward-looking statements that reflect current views with respect to, among other things, operations and financial performance.  Forward-looking statements include all statements that are not historical facts such as our statements about our expected financial results and guidance and our expectations for future business prospects.  In some cases, you can identify these forward-looking statements by the use of words such as “outlook,” “guidance,” “believes,” “expects,” “potential,” “continues,” “may,” “will,” “should,” “could,” “seeks,” “predicts,” “intends,” “plans,” “estimates,” “anticipates” or the negative version of these words or other comparable words.  Such forward-looking statements are subject to various risks and uncertainties including, among other things: our ability to achieve or sustain profitability in the future; our ability to demonstrate to spine surgeons the merits of our products; pricing pressures and our ability to compete effectively generally; collaboration and consolidation in hospital purchasing; inadequate coverage and reimbursement for our products from third-party payors; lack of long-term clinical data supporting the safety and efficacy of our products; dependence on a limited number of third-party suppliers; our ability to maintain and expand our network of direct sales employees, independent sales agencies and international distributors and their level of sales or distribution activity with respect to our products; proliferation of physician-owned distributorships in our industry; decline in the sale of certain key products; loss of key personnel; our ability to enhance our product offerings through research and development; our ability to manage expected growth; our ability to successfully acquire or invest in new or complementary businesses, products or technologies; our ability to educate surgeons on the safe and appropriate use of our products; costs associated with high levels of inventory; impairment of our goodwill and intangible assets; disruptions in our main facility or information technology systems;  our ability to ship a sufficient number of our products to meet demand; our ability to strengthen our brand; fluctuations in insurance cost and availability; our ability to comply with extensive governmental regulation within the United States and foreign jurisdictions; our ability  to maintain or obtain regulatory approvals and clearances within the United States and foreign jurisdictions; voluntary corrective actions by us or our distribution or other business partners or agency enforcement actions; recalls or serious safety issues with our products; enforcement actions by regulatory agencies for improper marketing or promotion; misuse or off-label use of our products; delays or failures in clinical trials and results of clinical trials; legal restrictions on our procurement, use, processing, manufacturing or distribution of allograft bone tissue; negative publicity concerning methods of tissue recovery and screening of donor tissue; costs and liabilities relating to environmental laws and regulations;  our failure or the failure of our agents to comply with fraud and abuse laws; U.S. legislative or Food and Drug Administration regulatory reforms; adverse effects of medical device tax provisions; potential tax changes in jurisdictions in which we conduct business; our ability to generate significant sales; potential fluctuations in sales volumes and our results of operations over the course of the year; uncertainty in future capital needs and availability of capital to meet our needs; our level of indebtedness and the availability of borrowings under our credit facility; restrictive covenants and the impact of other provisions in the indenture governing our convertible  senior notes and our credit facility;  continuing worldwide economic instability; our ability to protect our intellectual property rights; patent litigation and product liability lawsuits; damages relating to trade secrets or non-competition or non-solicitation agreements; risks associated with operating internationally; fluctuations in foreign currency exchange rates; our ability to comply with the Foreign Corrupt Practices Act and similar laws; increased costs and additional regulations and requirements as a result of being a public company; our ability to implement and maintain effective internal control over financial reporting; potential volatility in our stock due to sales of additional shares by our pre-IPO owners or otherwise; our lack of current plans to pay cash dividends; our ability to take advantage of certain reduced disclosure requirements and exemptions as a result of being an emerging growth company; potential dilution by the future issuances of additional common stock in connection with our incentive plans, acquisitions or otherwise; anti-takeover provisions in our organizational documents and our ability to issue preferred stock without shareholder approval; potential limits on our ability to use our net operating loss carryforwards; and other risks and uncertainties, including those described under the section entitled “Risk Factors” in our most recent Annual Report on Form 10-K filed with the SEC, as such factors may be updated from time to time in our periodic filings with the SEC, which are accessible on the SEC’s website at www.sec.gov.  Accordingly, there are or will be important factors that could cause actual outcomes or results to differ materially from those indicated in these statements.  These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included in this release and our filings with the SEC.

We operate in a very competitive and challenging environment.  New risks and uncertainties emerge from time to time, and it is not possible for us to predict all risks and uncertainties that could have an impact on the forward-looking statements contained in this release.  We cannot assure you that the results, events and circumstances reflected in the forward-looking statements will be achieved or occur, and actual results, events or circumstances could differ materially from those described in the forward-looking statements.

The forward-looking statements made in this press release relate only to events as of the date on which the statements are made.  We undertake no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as required by law.  We may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements and you should not place undue reliance on our forward-looking statements. Unless specifically stated otherwise, our forward-looking statements do not reflect the potential impact of any future acquisitions, mergers, dispositions, joint ventures, investments or other strategic transactions we may make.

Media Contact: Zeno Group on behalf of K2M Group Holdings, Inc. Christian Emering, 212-299-8985 Christian.Emering@ZenoGroup.com  Investor Contact: Westwicke Partners on behalf of K2M Group Holdings, Inc. Mike Piccinino, CFA, 443-213-0500 K2M@westwicke.com


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June 19, 2017 OrthoSpineNews

OR AKIVA, Israel, June 19, 2017 /PRNewswire/ —

Expanding Orthopedics Inc. (EOI), a medical device company focused on developing and commercializing innovative expandable devices for spine surgery, is proud to announce that Dr. Claudio Feler of the Cheyenne Regional Medical Group has adopted the FLXfit™ 3D Expandable TLIF Cage as his implant of choice for his MIS TLIF procedures. Dr. Feler noted that “Large bodies of clinical evidence show that lordotic restoration is crucial in addressing sagittal alignment. FLXfit’s™ unique articulating design allows for a very large implant footprint to pass through an MIS cannula and be positioned in the anterior portion of the disc space”.

Dr. Claudio Feler, Cheyenne Regional Medical Group and Associate Professor in the Department of Neurosurgery at the University of Tennessee Medical Center said, “The MIS FLXfit™ Inserter has been specifically designed to go through a narrow access tube and maintain clear line of sight while utilizing a microscope.” He added that “sagittal alignment improves outcomes and negates possible adjacent level disease. Functionally, patients tend to have less back pain postoperatively and less potential slip and falls as their horizontal gaze is corrected.” Dr. Feler concluded “FLXfit™ offers a superior approach for my surgical practice as the dial in lordosis is positioned optimally to help achieve sagittal alignment”.

Ofer Bokobza, CEO of EOI, says that “we are excited with our continued collaboration with Dr. Feler. As an early adopter in minimal invasive spine surgery and pioneer in interventional pain management, he recognizes the value of FLXfit™ for MIS surgery. His valued input has successfully helped us realize the new FLXfit™ MIS System”. Ofer emphasizes that “EOI recognizes the need for continuous innovation and the introduction of novel solutions through collaboration with leading surgeons. We believe that the FLXfit™ MIS system is raising the bar again and will help many surgeons transition to MIS spine surgery”.

About Expanding Orthopedics Inc.

Expanding Orthopedics Inc. is medical device company developing and marketing innovative products designed to address unmet clinical needs for spine care and improve long-term patients’ outcome. The Company is spearheaded by seasoned management team, and is advised by prominent spine surgeons. EOI owns a broad patent portfolio around anatomically fit, expandable devices for enhanced stability through MIS approach.

Contact info:
David Elkaim, VP Marketing and Sales
E-mail: david@xortho.com
Phone: (347) 3219683

SOURCE Expanding Orthopedics Inc.


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June 19, 2017 OrthoSpineNews

ATLANTA, June 19, 2017 /PRNewswire/ — Spine surgery offers a new lease on life for patients experiencing back pain and discomfort. With an estimated 450,000+ lumbar fusions performed each year in the United States, surgeons are familiar with Meditech Spine’s Talos® Lumbar Peek devices as essential components in the procedures they perform. And now Meditech offers surgeons the next generation of their already successful devices, the Talos® Lumbar (HA) Peek IBF that has received US Federal Drug Administration (FDA) 510(k) clearance to be marketed.

Surgeons treating patients with Degenerative Disc Disease (DDD), defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies, consider a lumbar decompression and fusion to help relieve symptoms in the spine. Meditech’s Talos® Lumbar (HA) Peek IBF device is an intervertebral body device intended for use in skeletally mature patients with DDD of the lumbar spine with up to Grade 1 spondylolisthesis at one or two contiguous levels from L2-S1. These devices are intended to be used with autograft and/or allograft comprised of cancellous and/or corticocancellous bone graft.

The Talos® Peek Lumbar IBF devices have been adopted and utilized throughout the US market since 2010. With this most recent FDA approval, Meditech will now market the Talos® lumbar interbodies with Invibio Biomaterial Solutions, PEEK-OPTIMA® HA Enhanced material.

PEEK-OPTIMA® HA Enhanced is a novel material for these interbody cages, contributing to the fusion process as it is strong, versatile and based on PEEK-OPTIMA® polymer compounded with hydroxyapatite (HA), a well-known osteoconductive material for enhancing bone apposition. This component is not a secondary surface coating or added texture but is completely integrated throughout the polymer and, consequently, throughout the implant and all surfaces. Since Meditech’s Talos®-C (HA) Cervical IBF clearance in 2015, Meditech and surgeons have observed similar results that mimic a preclinical ovine study that demonstrated better ongrowth and improved fusion when compared to Peek alone1 .

“We took a ‘wait and see’ approach with our introduction of HA Peek in our cervical implants in 2015,” says Eric Flickinger, co-founder of Meditech Spine. “With nearly two years of data, we saw enough clinical evidence and heard enough positive surgeon feedback to convince us to move our lumbar portfolio to this new technology. Bone ongrowth, and better and faster fusion outcomes are what surgeons look for in their patient follow up. This is exactly what we have seen, similar to the preclinical ovine study, with our cervical IBFs with PEEK-OPTIMA® HA Enhanced material.”

The Talos® HA Peek Lumbar System is a family of interbody devices that allows surgeons to choose their preferred method of approach for each patient whether it be a PLIF, TLIF, TPLIF, ALIF or LLIF. Meditech will introduce the six different lumbar IBF footprints of Talos®-P (HA), Talos®-P WB (HA), Talos®-T (HA), Talos®-TL (HA), Talos®-A (HA) and Talos®-L (HA) later this year. With this release, Meditech has added more footprints as well as hyperlordotic and asymmetric sizes to meet surgeons’ needs for their patients. The devices are designed with large graft windows to allow packing of autograft or allograft and come with disc preparation instruments to help facilitate and streamline the procedure. All the Talos® IBF implants will continue to be supplied in sterile packaging to aid in traceability and help reduce possible infection.

1.

Walsh WR, Pelletier MH, Bertollo N, Christou C, Tan C. Does PEEK/HA Enhance Bone Formation Compared With PEEK in a Sheep Cervical Fusion Model? Clin Orthop Relat Res. 2016; DOI 10.1007/s11999-016-4994-x

ABOUT MEDITECH SPINE

Meditech Spine, LLC, is a spinal implant company that 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. For more information visit www.meditechspine.com.

Caption & Copyright:
Talos® and Meditech logos are registered trademarks of Meditech Spine, LLC. All rights reserved. PEEK-OPTIMA® is a registered trademark of Invibio, Ltd. All rights reserved.

Meditech Spine, LLC
1447 Peachtree Street, Suite 440
Atlanta, GA 30309
Phone: 678-974-5287
Email: support@meditechspine.com

 

SOURCE Meditech Spine, LLC

Related Links

http://www.meditechspine.com


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June 16, 2017 OrthoSpineNews

June 16, 2017

LYON, France & NEW YORK–(BUSINESS WIRE)–The Medicrea Group (Alternext Paris: FR0004178572 – ALMED), pioneering the convergence of healthcare IT and next-generation, outcome-centered device design and manufacturing with UNiD™ ASI technology, announced today that it has received FDA 510(k) Clearance and performed first surgeries with PASS® TULIP top-loading fixation including world-first patient-specific hybrid constructs.

Top-loading fixation is the global standard for posterior spinal instrumentation. Medicrea’s PASS® TULIP provides a procedurally-integrated solution for surgeons to benefit from the Company’s UNiD™ ASI technology, a scientific, data-driven model for personalized spine care. The PASS® TULIP components are fully compatible with Medicrea’s PASS LP® to provide a unique hybrid approach in complex indications. The first-ever patient-specific hybrid spine surgery was successfully performed by Dr. Frank Schwab, Chief of Spine, at the Hospital for Special Surgery in New York.

“By using two compatible implant designs in a hybrid application, I am able to personalize a patient’s operation in a whole new way. The increased flexibility and precision help me to best achieve the patient’s optimal spinal alignment targeted by Medicrea’s patient-specific implants,” stated Dr. Schwab, who uses UNiD™ ASI technology to strategically plan cases supported by the UNiD™ LAB team. “Having these additional tools to achieve my surgical strategy translates to better alignment post-operatively and that’s clearly been shown to correlate with patient satisfaction and with long-term benefits of surgery.”

Denys Sournac, President and CEO, stated, “We are pleased to extend our distinctive Lifetime Warranty covering UNiD™ Rod constructs to include associated PASS® TULIP components.” Mr. Sournac continued, “The addition of PASS® TULIP to our comprehensive implant range will open new doors for Medicrea to gain market share for our UNiD™ ASI technology by lowering the barrier to entry for the large number of surgeons trained on top-loading instrumentation.”

PASS® TULIP components are differentiated from traditional top-loading implants by a thoughtful proprietary design that allows a single implant to perform multiple clinical functions through a simple one-step maneuver. The anticipated result is increased surgical efficiency in implant placement as well as a reduction in the inventory required for a case and associated processing costs.

About Medicrea (www.Medicrea.com)

Through the lens of predictive medicine, Medicrea leads the design, integrated manufacture, and distribution of 30+ FDA approved implant technologies, utilized in over 100k spinal surgeries to date. Operating in a $10 billion marketplace, Medicrea is an SME with 160 employees worldwide, which includes 55 at its USA Corp. subsidiary in NYC. The Company has an ultra-modern manufacturing facility in Lyon, France, housing the development and production of 3D-printed titanium patient-specific implants.

By leveraging its proprietary software analysis tools with big data and machine learning technologies supported by an expansive collection of clinical and scientific data, Medicrea is well-placed to streamline the efficiency of spinal care, reducing procedural complications and limiting time spent in the O.R.

For further information, please visit: Medicrea.com.

Connect with Medicrea:
FACEBOOK | INSTAGRAM | TWITTER | WEBSITE | YOUTUBE

Medicrea is listed on
ALTERNEXT Paris
ISIN: FR 0004178572
Ticker: ALMED

Contacts

Medicrea
Denys Sournac
Founder, Chairman and CEO
dsournac@Medicrea.com
or
Fabrice Kilfiger
Chief Financial Officer
fkilfiger@Medicrea.com
Tel: +33 (0)4 72 01 87 87


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June 16, 2017 OrthoSpineNews

June 16, 2017

LYON, France & NEW YORK–(BUSINESS WIRE)–The Medicrea Group (Alternext Paris: FR0004178572 – ALMED), pioneering the convergence of healthcare IT and next-generation, outcome-centered device design and manufacturing with UNiD™ ASI technology, announced today that it has received 510(k) Clearance from the Food & Drug Administration for UNiD™ HUB, a data-driven digital portal for the Company’s Adaptive Spine Intelligence.

“It is our belief that data science and analytics are critical components of improved patient outcomes and efficiencies. For that reason, Medicrea has stepped into a space unoccupied by traditional device manufacturers: Software development and Artificial Intelligence,” stated Denys Sournac, President and CEO of Medicrea. “The UNiD™ HUB represents Medicrea’s ability to lead the Spine industry with breakthrough innovations by offering a unique forward-thinking and holistic approach to personalized spinal surgery.”

The UNiD™ HUB is designed to support the surgeon workflow, identify tendencies and correlations and build predictive modeling to drive intelligent strategic decisions and create personalized implant solutions for surgery. The UNiD™ HUB software also serves to enhance the existing proprietary IT utilized by Medicrea’s UNiD™ ASI platform for digital surgical planning to create a seamless communication channel between the Company’s UNiD™ LAB biomedical engineers and Surgeon users to deliver UNiD™ TEK, patient-specific spinal implants manufactured by Medicrea through proprietary rod bending and 3D printing techniques.

The digital communication portal opened with the introduction of UNiD™ HUB instantly creates a sticky, user-friendly environment for surgeons to track and manage their open cases in both snapshot and detailed views, access their complete history with post-operative analyses and dialogue with a dedicated biomedical engineer in real time. Future functionalities will become available alongside the software’s wide release planned in October of 2017, for Eurospine in Dublin, Ireland on the 11-13 October and at the annual meeting of the North American Spine Society, held 25-28 October in Orlando, Florida.

Mr. Sournac continued, “As a media tool for surgeons, we have received very positive feedback from our UNiD™ ASI customers who have seen beta versions of the software and we are now ready to make the UNiD™ HUB digital portal immediately available to them. The software integrates well with their clinical habits and enhances their experience with UNiD™ ASI technology.” Mr. Sournac added, “This new generation of software will be more than a communication tool for surgeons – It will grant surgeons access to the same data analytics and machine learning technology that is curated by our data scientists to use the UNiD™ HUB as an unparalleled research engine and networking platform.”

UNiD™ HUB has been developed in desktop and mobile applications and is accessible from medical offices as well as on the go. For a first look at the UNiD™ HUB, a video preview is available for viewing here.

About Medicrea (www.Medicrea.com)

Through the lens of predictive medicine, Medicrea leads the design, integrated manufacture, and distribution of 30+ FDA approved implant technologies, utilized in over 100k spinal surgeries to date. Operating in a $10 billion marketplace, Medicrea is an SME with 160 employees worldwide, which includes 55 at its USA Corp. subsidiary in NYC. The Company has an ultra-modern manufacturing facility in Lyon, France housing the development and production of 3D-printed titanium patient-specific implants.

By leveraging its proprietary software analysis tools with big data and machine learning technologies supported by an expansive collection of clinical and scientific data, Medicrea is well-placed to streamline the efficiency of spinal care, reducing procedural complications and limiting time spent in the O.R.

For further information, please visit: Medicrea.com.

Connect with Medicrea:
FACEBOOK | INSTAGRAM | TWITTER | WEBSITE | YOUTUBE

Medicrea is listed on ALTERNEXT Paris ISIN: FR 0004178572 Ticker: ALMED

Contacts

Medicrea
Denys Sournac
Founder, Chairman and CEO
dsournac@Medicrea.com
or
Fabrice Kilfiger,
Chief Financial Officer
fkilfiger@Medicrea.com
Tel: +33 (0)4 72 01 87 87


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June 15, 2017 OrthoSpineNews

EDINA, MN, June 13, 2017 /PRNewswire/ – Twin Cities Orthopedics

Dr. John Sherman has performed the first herniated disc repair at Twin Cities Orthopedics using the AnchorKnot® Tissue Approximation Kit.

As a renowned surgeon, recognized by Becker’s Spine Review for his contributions to the advancement of spine surgery, Dr. Sherman has long identified the need to provide herniated disc repair. “Many studies have shown the size of the disc defect correlates with poor outcomes” as such, “if the AnchorKnot® system can effectively reduce the size of the defect then it may be possible to have better procedural outcomes.”

At Twin Cities Orthopedics, micro discectomy procedures are among the most commonly performed procedures. In the 20+ years that Dr. Sherman has been practicing, a common question arises from his patients: “Patients ask me what will happen to the hole left behind in the disc. It is intuitive to them that something must be done to close the hole, but until now, that hasn’t been possible.” Having used the AnchorKnot® system to effectively repair the disc, Dr. Sherman may now have an answer for them. While the nature of the injury differs from patient to patient, Dr. Sherman adds “I would use the AnchorKnot® system not only for young patients, but for anyone who is diagnosed with a lumbar disc herniation and is deemed a suitable patient for herniated disc repair.”

Neil Godara, General Manager of Anchor Orthopedics, comments that “as we are providing the AnchorKnot® system to more hospitals, we are finding that many surgeons share Dr. Sherman’s assessment on the need for our technology for use in herniated disc repair procedures. We are focused on providing a holistic solution to improve the outcomes of discectomy procedures and to reduce the rate of re-hospitalizations. Ultimately, we are focused on delivering value to patients, physicians and the healthcare system.”

Twin Cities Orthopedics is one of the leading orthopedic practices in the country. As the official sports medicine provider for the Minnesota Vikings, and the naming rights partner for the new home of the Minnesota Vikings in Eagan at the Twin Cities Orthopedics Performance Center and the Twin Cities Orthopedics Stadium, Twin Cities Orthopedics will also be opening a new orthopedic clinic adjacent to these facilities in Spring 2018, demonstrating a strong commitment to providing world class orthopedic and sports medicine care to patients.

About Twin Cities Orthopedics

For more than 75 years, Twin Cities Orthopedics has proudly provided a full spectrum of orthopedic and sports medicine care, devoted to the diagnosis, treatment, rehabilitation and prevention of injuries and conditions that affect the body’s muscles, joints and bones. TCO’s 115 physicians provide superior quality care across 39 state-of-the-art facilities in the Twin Cities and western Wisconsin. Visit TCOmn.com to learn more.

About Anchor Orthopedics

Anchor Orthopedics XT Inc., the developer of the AnchorKnot® Tissue Approximation Kit, aims to provide surgeons with novel solutions that optimize procedures in disc repair in an effort to preserve the biomechanics of the patient and improve surgical outcomes. Our mission is to work closely with surgeons on all aspects of development to create clinical solutions that serve to improve the lives of patients around the world. Anchor Orthopedics XT Inc., located in Mississauga, Canada, is a subsidiary of Baylis Medical Company Inc.

Media Contact Person:
Ester Kwok
Global Product Manager
Anchor Orthopedics XT Inc.
Tel: 647-484-0662 ext 388
ekwok@anchorortho.com
http://www.anchorortho.com

PRM-00214 EN J-1 V-1 © Anchor Orthopedics XT Inc., 2017. Anchor Orthopedics XT and AnchorKnot® are trademarks and/or registered trademarks of Anchor Orthopedics XT Inc. in the USA and/or other countries. All other trademarks are the property of their respective owners. CAUTION: Federal Law (USA) restricts the use of these devices to or by the order of a physician. Before use, consult product labels and Instructions for Use for Indications for Use, Contraindications, Warnings, Precautions, Adverse Events and Directions for Use. The AnchorKnot® Suture Passer (2-0) is an accessory of the Anchor System. The Anchor System is indicated for visualization of the surgical field in any area of the body cut open during a surgical procedure. When used in the cervical, thoracic, or lumbar spine either from an anterior or posterior direction, for example, the Anchor Endoscope and accessories are intended to aid the surgeon’s visualization of the surgical area and allow him/her to perform any type of surgical spinal procedure such as herniated disc repair, visualization of the circumferential decompression of the nerve roots, aiding in the search and removal of nucleus material, spinal fusion, or insertion of spinal implants. Other examples of generic surgical use of the Anchor System would be for use in the knee, ankle, shoulder, hand, wrist, and temporomandibular joint (TMJ). Patents pending and/or issued.

SOURCE Anchor Orthopedics