CoreLink Announces Full Commercial Launch of Foundation™ 3D Printed Titanium Interbody Cage Systems

April 11, 2018

ST. LOUIS–(BUSINESS WIRE)–CoreLink, LLC, a fast growing, vertically integrated designer and manufacturer of spinal implant systems, announced the full commercial release of its Foundation 3D Interbody Cage Systems for cervical and lumbar fusions.

The titanium devices utilize additive manufacturing to create Mimetic Metal™ technology that mimics key characteristics of natural bone, featuring 100% open-pore architecture and micro roughened porosity with significant hydro-wicking properties.

The lumbar devices incorporate patent pending StrutSure™ technology featuring an asymmetric load sharing support structure with an interconnected lattice that is designed to provide the optimal balance between strength, stiffness, and stability. This unique to market support structure minimizes overall implant density, providing for good imaging characteristics. Internal testing shows the center of the Straight Foundation 3D Lumbar interbody has a modulus of elasticity less than PEEK which may reduce stress shielding and enable the benefits of Wolff’s Law in three key areas: the interface with the vertebral endplates, the central graft column, and inside the walls of the device itself.

“I love how these cages image, both intraoperative and post op, without the typical hardware-associated artifacts we are used to with metal cages,” commented Justin Owen M.D., neurosurgeon in Slidell, LA, on his experience with the Foundation 3D Cervical cages. “I appreciate the possibility of the endplates growing around the porous metal surfaces, which would seem to provide faster stabilization towards fusion before growing across the entire disc space. This is a great system, for me and my patients.”

After a limited initial launch, CoreLink has now released full commercial quantities of all three devices: Cervical, Straight Lumbar, and Curved Lumbar. They are individually prepacked sterile and available in variety of footprints and lengths.

“We are excited about F3D, because of the significant improvement in patient care expected, but also because it establishes CoreLink as a leader in additive manufacturing,” said Jay Bartling, CoreLink’s CEO.

About CoreLink

CoreLink, known as The Source for Spine™, internally designs and manufactures more than 99% of its broad portfolio of spinal implant systems and leverages this expertise through collaboration and a dedication to empowering the performance of its surgeons and the improvement of the lives of their patients.

Be a part of something at The Source.

www.corelinksurgical.com

Contacts

CoreLink, LLC
Matthew Linhardt, 888-349-7808
m.linhardt@corelinksurgical.com

OrtoWay to Publish Scientific Abstract on First Use of OrtoWell® Distractor Tool in a Lateral Corpectomy at ISASS18 Spinal Meeting in Toronto

STOCKHOLMApril 11, 2018 /PRNewswire/ —

OrtoWay AB, the Stockholm-based medical technology company, will present a scientific abstract at ISASS18 in Toronto, Ontario, Canada on April 11, 2018, documenting the clinical use of its OrtoWell® device for the first time in a lateral, minimally invasive surgical (MIS) fixation procedure. The CE-marked device, which is now approved for most anterior-approach surgeries, was used at the renowned Dreifaltigkeits-Krankenhaus Clinic in Cologne, Germany to position a spinal implant in a 39-year-old male patient suffering from inflammation in the L1 and L2 vertebra.

Three-step operation strategy
Submitted by Dr. Biren Desai, Head of Department Spine Surgery at the Cologne-based clinic, the ISASS18 abstract is entitled: Introduction to using a novel hydraulically powered system – OrtoWell® Distractor – to separate vertebral bodies during anterior surgery: Case report of a spine inflammation with need for 2-level corpectomy, vertebral body replacement and fusion. Commenting on the scientific paper, he says: “We adopted a three-step surgical strategy involving an anterior lateral procedure to replace the L1 and L2 vertebra and then connect a Th-L plate from Th12 and L3 vertebra followed by posterior MIS fixation.”

Accurate positioning and fixation
According to Dr. Desai, the decision to use the OrtoWell® distractor tool was based on a desire to gain more freedom of working space, ensure smooth separation of the vertebra and support accurate fixation. “When replacing vertebra in the lumbar spine, it’s important to have tools that are easy to use and support accurate positioning and holding strength,” he says. “Not only did the OrtoWell® device help simplify the operation but I was impressed by the very strong, smooth hydraulic operation.” His clinic specializes in spine surgery, orthopedics and sports traumatology, treating 19,000 patients a year and carrying out more than 4,000 operations.

Resisting spinal compression forces
OrtoWell® was developed in Sweden by biomaterial and spinal experts who were looking for better tools to overcome the challenges of strong spinal compression forces, avoid the risk of damage to vertebra using hammers and other tools and improve accuracy. The system consists of several non-disposable components (distractor unit, spanner unit, retractor and frame, tools) as well as disposable components (tube unit, gauge, hooks, bone screws).

Strong and smooth hydraulics
“The use of gentle, yet powerful incremental hydraulic force to prevent the vertebrae from collapsing or moving during operation is beneficial to surgeons since it facilitates accurate positioning of spinal prosthetics such as disc implants and ALIF cages,” says Stan Mikulowski, CEO of OrtoWay AB, who adds: “In addition to corpectomies, the reliable distraction of vertebra can support a wide range of spinal procedures, including tumor removal, disc removal and artificial disc replacement, ALIF and scoliosis.”

CE Marked for Europe; FDA approved
The OrtoWell® device, which is CE Marked for Europe and FDA approved (Class 1 medical device). The company is currently performing a clinical trial program together with several clinics in Germany.

Many potential application areas
“We see many potential areas where the OrtoWell device could be a big support to spinal surgeons,” says Mr. Mikulowski. “The entire team at OrtoWay is strongly committed to improving patient outcomes with the help of superior spinal technology.”

About OrtoWay AB
OrtoWay AB was founded in 2007 by a group of experts in biomaterials, spinal surgery and medical technology who were looking for ways to improve anterior surgery and implantation of spinal prosthesis in the lumbar region. The developer behind the OrtoWell Distractor system, OrtoWay AB is today a Swedish privately held medical technology company that is seeking partners for commercialization. The OrtoWell instrument has CE marking for medical devices in Europe and is approved for usage as a Class 1 medical device in the USA. The product will be made available through OrtoWay LLC, an independent company based near Philadelphia, Pennsylvania, USA.

About ISASS
The International Society for the Advancement of Spine Surgery (ISASS) is a nonprofit scientific and educational society organized to discuss and assess existing strategies and innovate ideas in the clinical and basic sciences related to spine surgery to enhance patient care. Headquartered in New York, the organization partners with physicians, patients and the medical industry to advocate for high-quality, widely accessible and cost-effective spine care for patients around the world.

OrtoWay has received patents for this invention in Europe, the USA and in Australia.
OrtoWell® is a registered trademark in the USA, EU and Australia.
Currently OrtoWay is looking for partners to commercialize this invention.

Contact:

The receive a copy of the scientific paper or discuss possible collaborations, please contact:
Stan Mikulowski,
CEO / Partner/ Owner, OrtoWay LLC, PA, USA
Stan.mikulowski@ortoway.com

Cell phone: +46-708-769-991, From the US; 011-708-769-991
www.ortoway.com

This information was brought to you by Cision http://news.cision.com
http://news.cision.com/ortoway-ab/r/ortoway-to-publish-scientific-abstract-on-first-use-of-ortowell–distractor-tool-in-a-lateral-corpec,c2489214

The following files are available for download:

 

SOURCE OrtoWay AB

Related Links

http://www.ortoway.com

Titan Spine® Announces Review of Research Supporting Its nanoLOCK® Titanium Spinal Implants Published in SPINE

April 11, 2018

MEQUON, Wis.–(BUSINESS WIRE)–Titan Spine®, a medical device surface technology company focused on developing innovative spinal interbody fusion implants, today announced that a review of research supporting its nanoLOCK® surface technology has been published in the journal SPINE. nanoLOCK® is the company’s next-generation surface technology featuring enhanced micro and nano-scaled architecture, proven to significantly improve the osteogenic response it creates.It is the only technology with an FDA-nano-clearance and the only technology with a Centers for Medicare & Medicaid Services (CMS) new technology category designation for a nanotechnology surface.

The supplement article, “Spine Implant Surface Technology State of the Art: Separating Fact from Fiction,” authored by Titan Spine® Chief Medical Officer Paul J. Slosar, M.D., reviews the distinctive differences demonstrated among various types of spinal implant surface technologies, including those developed through additive (coating/3D printing) methods, subtractive methods, and of various materials including polyetheretherketone (PEEK), titanium and combination plasma-sprayed materials.

The review of research shows that the Company’s titanium nanotextured (10–9m) surface, engineered through a proprietary subtractive process, directly interacts with cells on a molecular level to generate specific cellular responses to drive bone production that porous or micron-scale (10–6m) implant surfaces cannot. Furthermore, it shows that the combination of the implant material and the nano-scale surface is critical to the ability to stimulate bone formation.

Dr. Slosar commented, “There has been a substantial increase in the promotion of surface-enhanced interbody devices over the past few years, most of which are backed by unsubstantiated marketing claims rather than by science. I felt the time was right to review the previously-published studies that point to one irrefutable fact – the only way to communicate to a patient’s cells in a meaningful way to drive bone growth is to combine titanium and the correct nano-architecture that only Titan Spine’s nanoLOCK®surface possesses. We are just now starting to produce clinical outcome data to determine if faster patient healing can be tied to the in-vitro findings summarized in this most-recent article. We look forward to publishing the data in the near future.”

The Company will be available to discuss these results at Titan Spine® Booth #401 during the 2018 International Society for the Advancement of Spine Surgery (ISASS) Annual Meeting, being held April 11 – 13 in Toronto, Canada.

Titan Spine® offers a full line of Endoskeleton® titanium implants that feature its proprietary nanoLOCK® surface technology, which was launched in the U.S. in October 2016 following FDA clearance in late 2014. The nanoLOCK® surface technology consists of a unique combination of roughened topographies at the macro, micro, and nano levels (MMN™). This unique combination of surface topographies is designed to create an optimal host-bone response and actively participate in the fusion process by promoting the upregulation of osteogenic and angiogenic factors necessary for bone growth, encouraging natural production of bone morphogenetic proteins (BMPs), downregulating inflammatory factors, and creating the potential for a faster and more robust fusion.2,3,4 All Endoskeleton® devices are covered by the company’s risk share warranty.

About Titan Spine®

Titan Spine®, LLC is a surface technology company focused on the design and manufacture of interbody fusion devices for the spine. The company is committed to advancing the science of surface engineering to enhance the treatment of various pathologies of the spine that require fusion. Titan Spine®, located in Mequon, Wisconsin and Laichingen, Germany, markets a full line of Endoskeleton® interbody devices featuring its proprietary textured surface in the U.S., portions of Europe, and Australia through its sales force and a network of independent distributors. To learn more, visit www.titanspine.com.

1 Olivares-Navarrete, R., Hyzy S.L., Gittens, R.A., Berg, M.E., Schneider, J.M., Hotchkiss, K., Schwartz, Z., Boyan, B. D. Osteoblast lineage cells can discriminate microscale topographic features on titanium-aluminum-vanadium surfaces. Ann Biomed Eng. 2014 Dec; 42 (12): 2551-61.

Olivares-Navarrete, R., Hyzy, S.L., Slosar, P.J., Schneider, J.M., Schwartz, Z., and Boyan, B.D. (2015). Implant materials generate different peri-implant inflammatory factors: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors. Spine, Volume 40, Issue 6, 399–404.

Olivares-Navarrete, R., Gittens, R.A., Schneider, J.M., Hyzy, S.L., Haithcock, D.A., Ullrich, P.F., Schwartz, Z., Boyan, B.D. (2012). Osteoblasts exhibit a more differentiated phenotype and increased bone morphogenetic production on titanium alloy substrates than poly-ether-ether-ketone. The Spine Journal, 12, 265-272.

4 Olivares-Navarrete, R., Hyzy, S.L., Gittens, R.A., Schneider, J.M., Haithcock, D.A., Ullrich, P.F., Slosar, P. J., Schwartz, Z., Boyan, B.D. (2013). Rough titanium alloys regulate osteoblast production of angiogenic factors. The Spine Journal, 13, 1563-1570.

Contacts

Company
Titan Spine
Andrew Shepherd, 866-822-7800
ashepherd@titanspine.com
or
Media
The Ruth Group
Kirsten Thomas, 508-280-6592
kthomas@theruthgroup.com

 

RTI Surgical® Showcases SImmetry® System Data and TETRAfuse® 3D Technology at ISASS 2018

April 11, 2018

ALACHUA, Fla.–(BUSINESS WIRE)–RTI Surgical, Inc. (Nasdaq: RTIX), a global surgical implant company, presented data on the SImmetry Sacroiliac Joint Fusion System at the International Society for the Advancement of Spine Surgery (ISASS) 2018 Annual Meeting taking place April 11-13, 2018 in Toronto, Canada. Data show the SImmetry System, the only minimally-invasive surgical procedure that promotes SI joint fusion through decortication, results in significant improvements in pain, disability and opioid use in patients suffering from SI joint dysfunction. RTI is also featuring the Fortilink®-C IBF System, the first in a series of devices to incorporate its TETRAfuse 3D Technology, used as an interbody fusion device in anterior cervical discectomy and fusion (ACDF) surgeries.

“These data add to the growing body of evidence supporting the SImmetry System as an innovative therapy for SI joint pain,” said Camille Farhat, President and CEO, RTI Surgical. “We look forward to sharing these data on the SImmetry System at ISASS, as well as showcasing Fortilink-C with TETRAfuse, our 3D-printed technology with unique features designed to enhance osseointegration and new bone formation.”

SImmetry Data: “Minimally Invasive Sacroiliac Joint Fusion Surgery with Decortication and Threaded Implants: Analysis of the EVoluSIon Clinical Study”

Dr. Ali Araghi from the Core Institute in Phoenix, Arizona, presented six-month clinical outcomes from 100 patients in the ongoing EVoluSIon Clinical Study. The EVoluSIon study is evaluating the impact of the SImmetry System on SI joint fusion and pain reduction in up to 250 patients at up to 40 sites. More than 200 patients have been enrolled to date.

Results showed the SImmetry System provided a 56 percent reduction in patient-reported pain, and a statistically significant reduction in the use of opioids and other pain medications at six months. The study also found a statistically significant improvement in disability and quality of life. These study results add to the growing body of evidence on the effectiveness of the SImmetry System and are consistent with the initial analysis published in December 2017.i

“We’re pleased to see these results – improvements in pain, disability, and opioid use – are consistent with earlier reported evidence,” Dr. Araghi commented. “We look forward to conducting longer term follow-up to evaluate continued pain reduction, hence an improved quality of life in our patients, as well as associated radiographic fusion rates.”

RTI Features Comprehensive Spine Portfolio at ISASS

RTI will showcase its comprehensive spine portfolio at Booth #412. A key feature will be the Fortilink-C IBF System with TETRAfuse 3D Technology. The Fortilink-C IBF System is the first 3D printed polymer-based, cervical interbody device featuring a nano-roughii surface with antibacterial characteristics†iii uniquely combined in one radiolucent bone-like material.ii The TETRAfuse 3D Technology is designed to participate in fusioniv without compromising mechanical integrityii or radiographic visibility,iisuggesting the Fortilink-C IBF System may be an important new option for surgeons commonly using titanium, allograft bone and PEEK systems.

The Fortilink-C IBF System has been available since October 2017. RTI is expanding its Fortilink series featuring TETRAfuse 3D Technology, aiming to launch new offerings later in 2018.

About RTI Surgical, Inc.

RTI Surgical is a leading global surgical implant company providing surgeons with safe biologic, metal and synthetic implants. Committed to delivering a higher standard, RTI’s implants are used in sports medicine, general surgery, spine, orthopedic and trauma procedures and are distributed in nearly 50 countries. RTI has four manufacturing facilities throughout the U.S. and Europe. RTI is accredited in the U.S. by the American Association of Tissue Banks and is a member of AdvaMed. For more information, please visit www.rtix.com.

Forward-Looking Statements

This communication contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are based on management’s current expectations, estimates and projections about our industry, our management’s beliefs and certain assumptions made by our management. Words such as “anticipates,” “expects,” “intends,” “plans,” “believes,” “seeks,” “estimates,” variations of such words and similar expressions are intended to identify such forward-looking statements. In addition, except for historical information, any statements made in this communication about anticipated financial results, growth rates, new product introductions, future operational improvements, gaining market share and results or regulatory actions or approvals or changes to agreements with distributors also are forward-looking statements. These statements are not guarantees of future performance and are subject to risks and uncertainties, including the risks described in public filings with the U.S. Securities and Exchange Commission (SEC). Our actual results may differ materially from the anticipated results reflected in these forward-looking statements. Copies of the company’s SEC filings may be obtained by contacting the company or the SEC or by visiting RTI’s website at www.rtix.com or the SEC’s website at www.sec.gov.

______________

i Araghi A et al. Pain and Opioid use Outcomes Following Minimally Invasive Sacroiliac Joint Fusion with Decortication and Bone Grafting: The Evolusion Clinical Trial. Open Orthop J. 2017;11:1440-1448.
ii Data on file at RTI Surgical, Inc.
iii Wang M, Bhardwaj B, Webster T; Antibacterial properties of PEKK for orthopedic applications. Int’l Journal of Nanomedicine. 2017: 12 6471-6476.
iv Data on file at RTI Surgical, Inc. Performance data from animal studies may not be representative of performance in humans.

Lab data may not be representative of the effects with all bacteria or performance when implanted in humans. Staphyloccocus epidermidis and Pseudomonas aeruginosa were subject bacterial strains in this study.

Please refer to the labeling for clinical applications, warnings, precautions and other instructions for use.

Contacts

RTI Surgical, Inc.
Media Contacts
Annie Claggett, +1-312-995-2856
aclaggett@rtix.com
or
Molly Poarch, +1-224-287-2661
mpoarch@rtix.com
or
Investor Contact
Nathan Elwell, +1-847-530-0249
nelwell@lincolnchurchilladvisors.com

Implanet Partners with the SRS

April 10, 2018

BORDEAUX, France & BOSTON–(BUSINESS WIRE)–Regulatory News:

Implanet (Paris:ALIMP) (OTCQX:IMPZY) (Euronext Growth: ALIMP, FR0010458729, eligible for PEA-PME equity savings plans; OTCQX: IMPZY), a medical technology company specializing in vertebral and knee-surgery implants, is announcing its participation at the next Scoliosis Research Society (SRS) course in Bordeaux. JAZZ will be presented in a workshop on restoring sagittal alignment.

Implanet will participate in the first course of the year held by the SRS in conjunction with EUROSPINE, which will run from April 12 to 14, 2018 at the Centre de Congrès Cité Mondiale in Bordeaux.

The course on “Current Concepts in Spine Deformity” will host surgeons from around the world.

Dr. Kariman Abelin-Genevois will lead the “Influence of Band Connectors on Sagittal Alignment Restoration” workshop at 5:15pm on Thursday April 12 in the Brasilia 3 room. Implanet’s JAZZ platform will be featured in this workshop.

Come and meet Implanet’s team at Stand #3 in the Exhibition Hall.

Next press release: First-quarter 2018 revenues on Tuesday April 24, 2018

About Scoliosis Research Society (SRS)

Founded in 1966, the Scoliosis Research Society is a society aimed at fostering optimal care for all patients with spinal deformities. Furthermore to its annual conference, the SRS coordinates regional courses to meet orthopaedics and neurosurgeons’ needs, who have undergone specialized training and who are performing spinal surgery and have an interest in surgery treatment and non-surgical treatment of patients with spinal deformities. This regional course is the first of the year 2018 out of a total of 5 courses, and should gather 55 spine specialists.

About IMPLANET

Founded in 2007, IMPLANET is a medical technology company that manufactures high-quality implants for orthopedic surgery. Its flagship product, the JAZZ® latest-generation implant, aims to treat spinal pathologies requiring vertebral fusion surgery. Protected by four families of international patents, JAZZ® has obtained 510(k) regulatory clearance from the Food and Drug Administration (FDA) in the United States and the CE mark. IMPLANET employs 48 staff and recorded 2017 sales of €7.8 million. For further information, please visit www.implanet.com.

Based near Bordeaux in France, IMPLANET established a US subsidiary in Boston in 2013.

IMPLANET is listed on Euronext™ Growth market in Paris. The Company would like to remind that the table for monitoring the BEOCABSA, OCA, BSA and the number of shares outstanding, is available on its website: http://www.implanet-invest.com/suivi-des-actions-80

Contacts

IMPLANET
Ludovic Lastennet, +33 (0)5 57 99 55 55
CEO
investors@implanet.com
or
NewCap
Investor Relations
Julie Coulot, +33 (0)1 44 71 20 40
implanet@newcap.eu
or
NewCap
Media Relations
Nicolas Merigeau, +33 (0)1 44 71 94 98
implanet@newcap.eu
or
AlphaBronze
US-Investor Relations
Pascal Nigen, +1 917 385 21 60
implanet@alphabronze.net

Ortho Sales Partners Announces the Addition of Chris Lyons as Vice President of Exit Strategy

Ortho Sales Partners, the global leader in commercialization services for the orthopedic industry, is pleased to announce a tremendous addition to the executive team. In an effort to serve clients from inception through exit, Ortho Sales Partners has recruited Chris Lyons to serve as its Vice President of Exit Strategy. Mr. Lyons will be a vital component of any client’s project as he will help create and guide the overall strategy and work on client’s behalf during possible transaction discussions.

Mr. Lyons career began at Smith and Nephew in 1989. While at SNN, he held numerous marketing roles, driving product launches, engaging surgeons, and creating intellectual property predominantly in the companies Knee and Hip product lines.  Additionally, he spent two years in the Smith and Nephew Sales Force to learn the underpinnings of what made the organization successful.

In 2005, Chris joined Medtronic Spine and Biologics, with the first three years being focused on driving growth of the International biologics business of Medtronic.  The opportunity presented itself to move into the realm of Business Development where he served the past 10 years. During this time, Mr. Lyons worked with all of the executive and cross functional leadership to transact various acquisitions, minority investments, as well as license and distribution agreements.  Chris was also selected to join the Board of the Southeast Medical Device Association (SEMDA) of which he remains a contributor, also serving as Chairman of the board for SEMDA for 2016.

With a highly driven, passionate, and entrepreneurial spirit, Chris is excited to be joining the ranks of Ortho Sales Partners as Vice President of Exit Strategy to assist this growing team of industry experts to influence positive commercialization and exit outcomes for Med Tech and Device companies. Chris will work closely with Venture Capital, Private Equity  and other companies focused on successfully exiting. Chris can provide Strategic Guidance, Gap Analysis, M&A consultation and will help implement general strategies that help the shareholders to maximize their return during due diligence and negotiations.

About his new role, Chris Lyons said: “The power of Ortho Sales Partners is their leadership. They have developed a game changing business based on integrity to positively influence better outcomes for medical device companies, which in turn has the possibility to influence greater innovation and healthcare delivery to the market in a timely manner.  I am excited to be part of this team of industry experts.”

“Chris Lyons is extremely well respected and we are thrilled that he has chosen to join our team of the industries most talented and experienced leaders. Ortho Sales Partners continues to demonstrate its commitment to excellence and our team has just gotten demonstrably stronger. We are now able to help companies successfully navigate from early commercialization through exit.” Said Kevin McGann, CEO of Ortho Sales Partners.

About Ortho Sales Partners

Ortho Sales Partners has created a unique platform to help companies in any stage commercialize their products in a very efficient way. We have worked closely with many organizations and produced results that have profoundly impacted each client’s business.

Our services are geared to meet you where you are today and help your business grow by utilizing proven industry executives that bring you an objective analysis and recommendations going forward. Our market knowledge is based on current trends and competitive analysis from industry stalwarts from some of the highest growth companies.

Ortho Sales Partners’ headquarters are in Scottsdale, Arizona but we have several offices across the US. (http://www.orthosalespartners.com).

 

SI-BONE, Inc. Hosts ISASS 2018 Sacroiliac Joint Workshop led by David Polly, MD, Bengt Sturesson, MD, Peter Whang, MD and Brad Duhon, MD

SAN JOSE, Calif.April 9, 2018 /PRNewswire/ — SI-BONE, Inc., a medical device company that pioneered minimally invasive surgical (MIS) treatment of the sacroiliac (SI) joint with the iFuse Implant System® (“iFuse”) announced that the company is a Silver Sponsor of the International Society for the Advancement of Spine Surgery (ISASS) 2018 Annual Conference in Toronto and will host an educational lunch workshop on the latest developments in diagnosis and treatment of the SI joint including recent commercial insurance coverage policies for MIS SI joint fusion with iFuse.  The workshop will take place on Thursday, April 12th from noon to 1:30 pm in Room 801A and will feature presentations by leaders in the field of spine surgery: David Polly, MD – University of Minnesota, Bengt Sturesson, MD – Angelholm Hospital in SwedenPeter Whang, MD – Yale School of Medicine and Brad Duhon, MD – University of Colorado.

“Leading the session are four distinguished and highly respected academic spine surgeons from the U.S. and Europe with decades of experience diagnosing and treating patients with SI joint disorders,” said Tony Recupero, Chief Commercial Officer at SI-BONE.  “We encourage ISASS attendees to participate in the SI joint lunch workshop to learn about the latest developments in SI joint fusion, progress on diagnosis and important commercial insurance coverage updates.”

In addition to the workshop, SI joint diagnosis and treatment will be the focus of eight podium presentations, including a one-hour symposium, which will be part of the ISASS 2018 scientific program:

Wednesday, April 11th:

1.      2-year Outcomes after Minimally Invasive Sacroiliac Joint Fusion or Conservative Management; Results of a Randomized Controlled Trial
Speaker:  B. Sturesson
8:15 am, Hall F

2.      3-year Outcomes after Minimally Invasive Sacroiliac Joint Fusion:  Prospective Multicenter Study
Speaker: P. Whang
9:28 am, Hall F

3.      Patients with Sacroiliac Joint Pain have Slower Walking Speeds and Shorter, Wider Gait than Healthy Controls
Speaker:  S. Kutz
10:30 am, Hall F

4.      Fixation of the Sacroiliac Joint:  A comparative anatomical analysis of the Lateral and Posterolateral Trajectories
Speaker:  B. Cheng
5:51 pm, Room 803B

5.      Coupled Translational Movements of the Sacroiliac Joint: An In-vitro Study
Speaker:  K. Odeh
5:53 pm, Room 803B

Thursday, April 12th:
6.      Neuromuscular Activity during Gait in Patients with Sacroiliac Joint Pain Compared to Healthy Controls
Speaker:  J. Cox
10:55 am, Hall F

7.      Symposium 3: The Sacroiliac Joint – The Pathway from Pain to Treatment
Moderators: M. Lorio, F. Phillips
5:00 pm – 6:00 pm, Hall F

Friday, April 13th:
8.      Off-Axis Rotation of the Sacroiliac Joint: An In-vitro Study
K. Odeh
2:45 pm, Hall F

Conference attendees can visit SI-BONE booth #400 to learn more about the latest advances in SI joint diagnosis, treatment and insurance coverage for SI joint fusion using the iFuse Implant System.

About SI joint dysfunction
The SI joint has been attributed as a source of pain in 15-30 percent of patients with chronic low back pain1-4, and in up to 43 percent of patients with new onset or persistent low back pain after lumbar fusion.5  SI joint dysfunction is often misdiagnosed and the resulting pain can be incorrectly attributed to other causes.  SI joint dysfunction can be identified when a patient points to the source of their pain directly over the posterior superior iliac spine (PSIS), known as the Fortin Finger Test6, combined with a number of positive provocative maneuvers that stress the SI joint and elicit pain, followed by image-guided diagnostic injections to confirm the diagnosis.  The SI joint is the largest of the eight major joints in the human body and the last to have a proven surgical treatment.  The iFuse Implant, first FDA-cleared in 2008, is the only device for treatment of certain causes of SI joint dysfunction supported by significant published clinical evidence, including level 1 trials, showing safety and durable effectiveness, including providing lasting pain relief.  The iFuse Implant was designed specifically to withstand the extreme forces resulting from load-bearing and the unique rotational and translational motion of the SI joint referred to as nutation, and has been the subject of more than 50 peer-reviewed publications, including two Level 1 randomized controlled trials (www.si-bone.com/results), published since its introduction to the market in 2009.

About SI-BONE, Inc.
SI-BONE, Inc. (San Jose, California) is a leading medical device company that developed the iFuse Implant System, a proprietary minimally invasive surgical implant system to fuse the sacroiliac joint to treat common disorders of the joint that can cause lower back pain.  Patients with certain types of sacroiliac joint dysfunction experience pain that can be debilitating.

The iFuse Implant System is intended for sacroiliac fusion for conditions including sacroiliac joint dysfunction that is a direct result of sacroiliac joint disruption and degenerative sacroiliitis.  This includes conditions whose symptoms began during pregnancy or in the peripartum period and have persisted postpartum for more than 6 months.  There are potential risks associated with the iFuse Implant System.  It may not be appropriate for all patients and all patients may not benefit.  For information about the risks, visit: www.si-bone.com/risks

One or more of the individuals referred to herein are investigators participating in clinical research sponsored by SI-BONE, paid consultants of SI-BONE and/or SI-BONE stockholders.

SI-BONE and iFuse Implant System are registered trademarks of SI-BONE, Inc.  ©2018 SI-BONE, Inc. All Rights Reserved. 10143.040918

  1. Bernard TN, Kirkaldy-Willis WH. Recognizing Specific Characteristics of Nonspecific Low Back Pain. Clin Orthop Relat Res. 1987;217:266–80.
  2. Schwarzer AC, Aprill CN, Bogduk N. The Sacroiliac Joint in Chronic Low Back Pain. Spine. 1995;20:31–7.
  3. Maigne JY, Aivaliklis A, Pfefer F. Results of Sacroiliac Joint Double Block and Value of Sacroiliac Pain Provocation Tests in 54 Patients with Low Back Pain. Spine. 1996;21:1889–92.
  4. Sembrano JN, Polly DW Jr. How Often is Low Back Pain Not Coming From The Back? Spine. 2009;34:E27–32.
  5. DePalma M, Ketchum JM, Saullo TR. Etiology of Chronic Low Back Pain Patients Having Undergone Lumbar Fusion. Pain Med. 2011;12:732–9.
  6. Fortin JD, Falco FJ. The Fortin finger test: an indicator of sacroiliac pain. Am J Orthop (Belle Mead NJ). 1997;26(7):477–480.

 

SOURCE SI-BONE, Inc.

Related Links

http://www.si-bone.com

SI-BONE, Inc. Announces Publication of 3-Year Long-term Prospective Outcomes Including Randomized Controlled Trial Data Post SI Joint Fusion with Triangular iFuse Implant System®

SAN JOSE, Calif.April 9, 2018 /PRNewswire/ — SI-BONE, Inc., a medical device company that pioneered the minimally invasive surgical (MIS) treatment of the sacroiliac (SI) joint with the iFuse Implant System® (“iFuse”) announced the publication of results from a long-term outcomes study called LOIS (Long Term Outcomes from INSITE and SIFI).  The publication, titled Long-term prospective outcomes after minimally invasive trans-iliac sacroiliac joint fusion using triangular titanium implants1 reports 3-year results of a subset of patients who participated in INSITE (Investigation of Sacroiliac Fusion Treatment)2, a U.S. randomized controlled trial and SIFI (Sacroiliac Joint Fusion with iFuse Implant System)3, a U.S. prospective multicenter trial.  The 3-year results from LOIS demonstrated that improvements in pain, function and quality of life achieved at 2-years were sustained at 3-years and patient satisfaction remained high for patients treated with the iFuse Implant, available in the US since 2009.  There were no reported adverse events related to the study device or procedure in the extended follow-up period.

The 3-year LOIS study results include 103 subjects at 12 medical centers with SI joint dysfunction due to degenerative sacroiliitis or SI joint disruption who were evaluated in study clinics at study start and at 3, 4 and 5 years follow-up.  3-year follow-up was 93%. Mean preoperative SI joint pain was 81.5 (0 to 100 VAS) and decreased to 26.2 at 3-years, a 55-point improvement (Figure 1).  Mean preoperative Oswestry Disability Index (ODI) was 56.3 and decreased to 28.2 at 3-years, a 28.1-point improvement (Figure 2).

“The 3-year LOIS results show that clinically significant improvements from both INSITE and SIFI patients were sustained at 3-years demonstrating that the benefits of SI joint fusion with iFuse are durable,” said Emily Darr, MD, Assistant Professor, Orthopaedic Surgery, Medical University of South Carolina College of Medicine and lead author on the publication.  “Furthermore, the diagnosis of SI joint mediated pain has been described as challenging, but our results suggest that SI joint dysfunction can be reliably diagnosed through appropriate history, physical exam and response to diagnostic block and can be effectively treated.”

“Based on the 56 peer-reviewed publications on iFuse,  fourteen (14) commercial payers have established positive coverage policies for MIS SI joint fusion exclusively for the triangular iFuse Implant System from SI-BONE and no other SI joint fusion implants are covered by those payers,” stated Daniel Cher, MD, Vice President of Clinical Affairs at SI-BONE.

About SI joint dysfunction
The SI joint has been attributed as a source of pain in 15-30 percent of patients with chronic low back pain4-7, and in up to 43 percent of patients with new onset or persistent low back pain after lumbar fusion.8  SI joint dysfunction is often misdiagnosed and the resulting pain can be incorrectly attributed to other causes.  SI joint dysfunction can be identified when a patient points to the source of their pain directly over the posterior superior iliac spine (PSIS), known as the Fortin Finger Test9, combined with a number of positive provocative maneuvers that stress the SI joint and elicit pain, followed by image-guided diagnostic injections to confirm the diagnosis.  The SI joint is the largest of the eight major joints in the human body and the last to have a proven surgical treatment.  The iFuse Implant, first FDA-cleared in 2009, is the only device for treatment of certain causes of SI joint dysfunction supported by significant published clinical evidence, including level 1 trials, showing safety and durable effectiveness, including providing lasting pain relief.  The iFuse Implant was designed specifically to withstand the extreme forces resulting from load-bearing and the unique rotational and translational motion of the SI joint referred to as nutation, and is supported by more than 50 peer-reviewed publications, including two Level 1 randomized controlled trials (www.si-bone.com/results).

About SI-BONE, Inc.
SI-BONE, Inc. (San Jose, California) is a leading medical device company that developed the iFuse Implant System, a proprietary minimally invasive surgical implant system to fuse the sacroiliac joint to treat common disorders of the joint that can cause lower back pain.  Patients with certain types of sacroiliac joint dysfunction experience pain that can be debilitating.

The iFuse Implant System is intended for sacroiliac fusion for conditions including sacroiliac joint dysfunction that is a direct result of sacroiliac joint disruption and degenerative sacroiliitis.  This includes conditions whose symptoms began during pregnancy or in the peripartum period and have persisted postpartum for more than 6 months.  There are potential risks associated with the iFuse Implant System.  It may not be appropriate for all patients and all patients may not benefit.  For information about the risks, visit: www.si-bone.com/risks

SI-BONE and iFuse Implant System are registered trademarks of SI-BONE, Inc. ©2018 SI-BONE, Inc. All Rights Reserved. 10133.032818

  1. Darr E, Meyer SC, Whang PG, Kovalsky D, Frank C, Lockstadt H, Limoni R, Redmond A, Ploska P, Oh MY, Cher D, Chowdhary A. Long-term Prospective Outcomes After Minimally Invasive Trans-Iliac Sacroiliac Joint Fusion Using Triangular Titanium Implants. Medical Devices: Evidence and Research. 2018:11;113-121. doi: 10.2147/MDER.S160989.
  2. Polly DW, Swofford J, Whang PG, Frank CJ, Glaser JA, Limoni RP, Cher DJ, Wine KD, Sembrano JN, and the INSITE Study Group. Two-Year Outcomes from a Randomized Controlled Trial of Minimally Invasive Sacroiliac Joint Fusion vs. Non-Surgical Management for Sacroiliac Joint Dysfunction. Int J Spine Surg. 2016;10:Article 28. doi: 10.14444/3028.
  3. Duhon BS, Bitan F, Lockstadt H, Kovalsky DA, Cher DJ, Hillen T, on behalf of the SIFI Study Group. Triangular Titanium Implants for Minimally Invasive Sacroiliac Joint Fusion: 2-year Follow-up from a Prospective Multicenter Trial. Int J Spine Surg. 2016;10:Article 13. doi: 10.14444/3013.
  4. Bernard TN, Kirkaldy-Willis WH. Recognizing Specific Characteristics of Nonspecific Low Back Pain. Clin Orthop Relat Res. 1987;217:266–80.
  5. Schwarzer AC, Aprill CN, Bogduk N. The Sacroiliac Joint in Chronic Low Back Pain. Spine. 1995;20:31–7.
  6. Maigne JY, Aivaliklis A, Pfefer F. Results of Sacroiliac Joint Double Block and Value of Sacroiliac Pain Provocation Tests in 54 Patients with Low Back Pain. Spine. 1996;21:1889–92.
  7. Sembrano JN, Polly DW Jr. How Often is Low Back Pain Not Coming From The Back? Spine. 2009;34:E27–32.
  8. DePalma M, Ketchum JM, Saullo TR. Etiology of Chronic Low Back Pain Patients Having Undergone Lumbar Fusion. Pain Med. 2011;12:732–9.
  9. Fortin JD, Falco FJ. The Fortin finger test: an indicator of sacroiliac pain. Am J Orthop (Belle Mead NJ). 1997;26(7):477–480.

 

SOURCE SI-BONE, Inc.

Related Links

http://www.si-bone.com

Premia Spine Features TOPS™ System and ProMIS™ Fixation System at ISASS Cadaver Lab

Philadelphia, PA, April 6, 2018 — Premia Spine, Ltd. announced today that it will sponsor a hands-on cadaver lab for participants at the International Society for the Advancement of Spine Surgery in Toronto.  The event will take place on Thursday, April 12th and feature both the ProMIS™ Fixation System and the TOPS™ System.  This will be the first time that surgeons in North America will have the opportunity to try both technologies in an open cadaver lab setting.

“I am very pleased to offer surgeons the opportunity to experience the advantages of our One-Step, direct Skin-to-Screw technique,” stated Tom O’Hara, recently appointed President of Premia Spine, Inc. “We are the first company to launch this patented approach—a technique that reduces x-ray exposure and saves screw placement time.”  Surgeons will also gain hands-on experience with other unique features to the ProMIS™ Fixation System.

In addition, Premia Spine will be offering surgeons a chance to work with the TOPS™ System—a posterior motion preservation system for patients with degenerative lumbar spondylolisthesis and spinal stenosis.  The TOPS System is approved in Europe and Australia, and under investigation in the United States.

Premia Spine launched the US IDE study among leading centers in the United States, including the Cleveland Clinic, Mayo Clinic, UPenn, UPMC Harrisburg, Carolina Neurosurgery, Ascension Jacksonville, Allegheny Health Network, Florida Spine Institute, Johns Hopkins-Sibley, and Wisconsin Bone and Joint.

“We want to showcase our solution before leading surgeons from around the world.  In addition, we are offering US surgeons the opportunity to join our IDE study—which still has a few remaining slots,” said Ron Sacher, CEO of Premia Spine.

The new TOPS device, with a 30% smaller footprint and a simpler surgical technique from the original device, has been in commercial use in Europe for over 6 years.

The IDE study will take place in 30 institutions and enroll 330 subjects.  Patients will be randomized to either the TOPS™ System or lumbar fusion (i.e., an interbody cage plus screws and rods), with a 67% likelihood of receiving the TOPS device.

Clinical sites will be measuring ODI, VAS, neurologic function, device integrity, reoperation rates and other quantitative outcomes for the study device and the fusion control.  “Our goal is to establish the superiority of the TOPS™ System versus traditional lumbar spinal fusion,” explains Mr. Sacher.

About Premia Spine.  Premia Spine licensed the TOPS System technology in 2011 from Impliant, Ltd. Over $100 million has been invested to design, develop, and commercialize the TOPS System, with over 12 years of clinical use and 1,000 patients.

Contact:
Ron Sacher, CEO

ronsacher@premiaspine.com

CTL Wins FDA Approval for Seurat Universal Pedicle Screw

DALLAS, TX / ACCESSWIRE / March 29, 2018 / CTL Medical Corporation, a Dallas-based medical device manufacturing and service company, has recently secured clearance and approval from the Food and Drug Administration to market its new SEURAT Universal Pedicle Screw System for the practice of spine fusion surgery. This is the second FDA clearance for the company in the first quarter of 2018. CTL Medical’s in-house research and development team designed the SEURAT Universal Pedicle Screw System after working closely with surgeons to determine the most comprehensive, adaptable, and advanced features for use in the surgical operative environment.

“The FDA approval of the SEURAT Universal Pedicle Screw System enables us to offer very versatile intraoperative hardware options for surgeons and the surgical spine industry as a whole,” stated Danny Chon, CEO for CTL Medical Corporation. “As the general population continues to age and the reported degenerative spine cases increase, it is inevitable that the pedicle screw market and related instrumentation challenges will continue to grow, ultimately demanding a one-stop solution. As an answer to this need, we designed the SEURAT Universal Pedicle Screw System to be a truly comprehensive pedicle screw offering unlike any other in the market today.”

The SEURAT Universal Pedicle Screws are medically classified as bone screws, designed for direct implantation into a vertebral pedicle. This system is a compilation and consolidation of the best features from each of CTL Medical’s already cleared pedicle screw systems, boasting the addition of true intraoperative versatility. The modular housing assembly option enables surgeons to intraoperatively build the most appropriate implant for the present indication, and the option to select a standard or reinforced-ring locking set screw ensures the SEURAT Universal Pedicle Screw System will accommodate a broader range of anatomical challenges and usage preferences. This comprehensive single system includes polyaxial and monoaxial; open and MIS; single and dual thread profile; solid and cannulated; and hex and hexalobe screws of all diameters and lengths.

CTL Medical expects to launch the SEURAT Universal Pedicle Screw System in the second half of 2018.

For more information on CTL Medical Corporation, visit www.ctlmed.com.

About CTL Medical Corporation

CTL Medical Corporation is a fully integrated, innovative, industry-leading, global medical device design, development and manufacturing company. CTL has assembled a world-class executive team, bringing together some of the industry’s most exceptional talents, positioning it to be a leader in medical device design and manufacturing. For more information, visit www.ctlmed.com.

Media Contact:

Jeff Cheatham
TrizCom PR
O: 972-247-1369
C: 972-961-6171
jeffc@trizcom.com

SOURCE: CTL Medical Corporation