100th Patient Enrolled in Clinical Trials for Active Implants’ NUsurface® Meniscus Implant

August 09, 2017

MEMPHIS, Tenn.–(BUSINESS WIRE)–Active Implants, LLC, a company that develops orthopedic implant solutions, today announced enrollment of the 100th patient in clinical trials evaluating the NUsurface® Meniscus Implant for the treatment of persistent knee pain caused by injured or deteriorating meniscus tissue. The surgery was performed by orthopedic surgeon Dr. Wayne Gersoff of Advanced Orthopedics & Sports Medicine Specialists in Denver, Co.

“Treating the 100th NUsurface patient in the U.S. is an important milestone for us as we continue on our mission to fulfill the unmet need in the orthopedic market,” said Ted Davis, president and CEO of Active Implants. “We are pleased that enrollment is going very well and expect to fully enroll all of the patients in the study plan in the coming months. Over the next two to three years, pending FDA clearance, we should be in a position to bring our product to market in the U.S. and fill the gap between minimally invasive meniscus repair and total knee replacement.”

If approved by the Food & Drug Administration, the NUsurface Implant would be the first “artificial meniscus.” The meniscus is a tissue pad between the thigh and shin bones, and once damaged, the meniscus in middle aged patients has a very limited ability to heal itself. Current treatment for a damaged or torn meniscus includes pain management, physical therapy, injections, repair techniques or meniscectomy. It has been estimated that from 700,000 to over 1 million partial meniscectomies are performed annually in the U.S. in an attempt to alleviate pain; however, recent studies have shown that many people who get a meniscectomy continue to experience pain that impacts their quality of life and can eventually lead to knee replacement surgery.

“The NUsurface Implant offers hope for patients who are experiencing persistent knee pain following meniscus injury and surgery, have exhausted non-surgical options and are not yet candidates for total knee replacement,” Dr. Gersoff said. “It’s encouraging to know that with this implant we may be able to alleviate pain and swelling, and delay or even avoid knee replacement surgery – allowing these patients to get back to activities they love.”

The NUsurface Meniscus Implant is made from medical grade polymer and, as a result of its unique materials, composite structure and design, does not require fixation to bone or soft tissues. The NUsurface Implant helps mimic the function of the natural meniscus and redistributes loads transmitted across the knee joint. The NUsurface Meniscus Implant has been used in Europe since 2008 and Israel since 2011.

Active Implants is sponsoring two clinical trials to support regulatory approval from the U.S. Food & Drug Administration (FDA): The VENUS (Verification of the Effectiveness of the NUsurface System) trial is a randomized, controlled study comparing the NUsurface Meniscus Implant compared to non-surgical standard of care and the SUN (Safety Using NUsurface) trial is a single-arm study assessing the safety and effectiveness of the NUsurface Meniscus Implant in restoring function similar to that of a natural, healthy meniscus. The clinical trials are continuing to enroll patients in the following U.S. cities:

VENUS Study

  • Albany, New York – Capital Region Orthopaedics (Richard Alfred, MD)
  • Boston, Massachusetts – Brigham and Women’s (Andreas Gomoll, MD) and New England Baptist (Brian McKeon, MD)
  • Columbus, Ohio – Ohio State University (Christopher Kaeding, MD)
  • Durham, North Carolina – Duke University Medical Center (William Garrett, Jr., MD and Claude T. Moorman III, MD)
  • Indianapolis, Indiana – OrthoIndy (Jack Farr, MD)
  • Memphis, Tennessee – OrthoMemphis (Randall Holcomb, MD)
  • New York, New York – Lenox Hill Hospital (Elliott Hershman, MD)
  • Richmond, Virginia – Advanced Orthopaedics (Kenneth Zaslav, MD)
  • Rochester, New York – University of Rochester Medical (Michael Maloney, MD)

SUN Study

  • Arlington, Texas – Baylor Orthopedic and Spine Hospital (Joseph Berman, MD)
  • Baton Rouge, Louisiana – Baton Rouge Orthopaedic Clinic (Brent Bankston, MD and Robert Easton, MD)
  • Boulder, Colorado – Colorado University Sports Medicine (Eric McCarty, MD)
  • Denver, Colorado – Advanced Orthopedics & Sports Medicine Specialists (Wayne Gersoff, MD)
  • Long Beach, California – Memorial Orthopaedic Surgical Group (Peter Kurzweil, MD)
  • New Orleans, Louisiana – Ochsner Sports Medicine Institute (Deryk Jones, MD)
  • Phoenix, Arizona – TOCA, The Orthopedic Clinic Association (Tom Carter, MD)
  • Portland, Oregon – Sports Medicine Oregon (Richard Edelson, MD and John Greenleaf, MD)
  • Salt Lake City, Utah – Salt Lake Regional Medical Center (Andrew Cooper, MD)
  • San Diego, California – Grossmont Orthopaedic Medical Group (Scott Hacker, MD)
  • San Francisco, California – St Mary’s Medical Center (William Montgomery, MD)

About Active Implants LLC

Active Implants LLC develops orthopedic implant solutions that complement the natural biomechanics of the musculoskeletal system, allowing patients to maintain or return to an active lifestyle. Active Implants is privately held with headquarters in Memphis, Tennessee. European offices are in Haarlem, The Netherlands, with R&D facilities in Netanya, Israel. For more information, visit www.activeimplants.com.

CAUTION Investigational device. Limited by United States law to investigational use.

Contacts

Merryman Communications
Joni Ramirez, 323-532-0746
joni@merrymancommunications.com

Knee surgery: Have we been doing it wrong?

August 7, 2017, MDLinx/University at Buffalo Health and Medicine News

Cleaning up loose cartilage is not always beneficial, according to a new University at Buffalo study that could impact athletes and seniors, reduce health care costs.
A team of University at Buffalo medical doctors has published a study that challenges a surgical practice used for decades during arthroscopic knee surgery.

When treating meniscal tears surgeons also have clipped and smoothed any dislodged cartilage they found in the belief it was helping patients. But the new study finds that practice does not benefit the patient. Patients who did not have dislodged cartilage removed, recovered faster, with less pain, and ended up a year later with identical results.

“Those with less surgery got better faster in comparison with the people we did more surgery on,” said Leslie J. Bisson, MD, professor and chair in the Department of Orthopaedics at the Jacobs School of Medicine and Biomedical Sciences at UB and lead author of the study.

The finding was so surprising that an editor at The Journal of Bone & Joint Surgery, which published the study, also published a commentary that said, “The conclusion that unstable cartilage lesions do not need debridement could have a dramatic impact on practice management, save health–care dollars, and improve early patient outcomes.”

The American Academy of Orthopaedic Surgeons also distributed the study on its weekly collection of papers of note.

 

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Grossmont Orthopaedic Medical Group Performs First Meniscus Replacement in San Diego with NUsurface® Meniscus Implant

July 25, 2017

SAN DIEGO–(BUSINESS WIRE)–Dr. Scott A. Hacker, an expert in arthroscopic surgery, total joint replacements, sports medicine and fracture care, and Active Implants, a company that develops orthopedic implant solutions, today announced that the first meniscus replacement procedure in San Diego has been performed. Dr. Hacker is the only physician in San Diego County – and Grossmont Orthopedic Medical Group is one of just 10 sites nationwide – enrolling patients with persistent knee pain caused by injured or deteriorating meniscus cartilage in the SUN trial, which is designed to assess the ability of the NUsurface® Meniscus Implant (pronounced “new surface”) in restoring function similar to that of a natural, healthy meniscus.

The recipient of the implant was Justin Marchand, 40-year-old Carlsbad resident and father of six. Four years ago, Marchand tore the meniscus in his left knee while practicing Brazilian Jiu-Jitsu drills, only to suffer a second tear in the same knee in 2014 while jogging. Although he underwent two partial meniscectomies to treat the tears, he continued to suffer from constant pain and swelling in his knee. As an avid surfer for over 25 years, Marchand went from surfing every day to once per week at best – with the expense of pain flare-ups after each session. His knee became extremely vulnerable to any type of sudden movement, and he was forced to limit all sports activities, including mountain biking, skiing and hiking.

The meniscus is a tissue pad between the thigh and shin bones. Once damaged, the meniscus has a very limited ability to heal. Over 1 million partial meniscectomies to remove or repair a torn meniscus are performed in the U.S. every year, about the same as the total number of hip and knee replacement surgeries combined. However, many patients still experience persistent knee pain following meniscus surgery.

“There aren’t many great options for patients like Justin, who experience persistent knee pain following meniscus surgery but are too young for knee replacement surgery,” Dr. Hacker said. “We hope the SUN study finds that the NUsurface implant alleviates pain in these patients, as well as helps them delay or avoid knee replacement surgery. Patients routinely ask me for something simple that could be put in the joint – this is that option they have been waiting for.”

Marchand received the NUsurface Meniscus Implant on July 25 in a short operation during which the implant was placed into his left knee joint through a small incision. He will now undergo a six-week rehabilitation program, after which time he can begin to resume work, leisure and sports activities.

“For the last four years, I had resigned myself to living with knee pain and limited mobility,” Marchand said. “As a father of six children, it has been particularly heartbreaking because I have not been able to go surfing with my kids or participate in the outdoor activities we love. I am hopeful that the NUsurface Implant will help me get back to my active lifestyle and allow me to go hiking with my family without persistent knee pain.”

The NUsurface Meniscus Implant has been used in Europe under CE Mark since 2008 and Israel since 2011.

About the Clinical Trial

The SUN study (Safety Using NUsurface®) will enroll approximately 120 patients as part of regulatory process to gain approval from FDA to sell the device in the U.S. All patients who meet study requirements and agree to enter the trial are offered the NUsurface Meniscus Implant as treatment. Treatment with NUsurface in the SUN trial is eligible for coverage by Medicare and some private insurance companies. To be eligible for the study, participants must be between the ages of 30 and 75 and have pain after medial meniscus surgery that was performed at least six months ago. To learn more about the SUN study, please visit http://sun-trial.com or call (844) 680-8951.

About the NUsurface® Meniscus Implant

The NUsurface® Meniscus Implant is an investigational treatment for patients with persistent knee pain following medial meniscus surgery. It is made from medical grade plastic and, as a result of its unique materials, composite structure and design, does not require fixation to bone or soft tissues. The NUsurface Meniscus Implant is intended to mimic the function of the natural meniscus and redistribute loads transmitted across the knee joint. Clinical trials are underway in the U.S., Europe and Israel.

About Grossmont Orthopaedic Medical Group

Grossmont Orthopedic Medical Group is a premier Orthopedic center in San Diego caring for patients throughout southern California. The orthopedic surgeons of Grossmont Orthopaedic Medical Group, are consistently voted as top doctors in their field. As a group they have advanced training in arthroscopic surgery, total joint replacements, sports medicine and fracture care. The doctors are actively involved in many cutting edge research techniques allowing them to care for a wide range of orthopedic problems tailored to the individual and their needs. Their training, dedication, and experience are the prescription for successful orthopaedic treatment.

About Active Implants LLC

Active Implants LLC develops orthopedic implant solutions that complement the natural biomechanics of the musculoskeletal system, allowing patients to maintain or return to an active lifestyle. Active Implants is privately held with headquarters in Memphis, Tennessee. European offices are in Haarlem, The Netherlands, with R&D facilities in Netanya, Israel. For more information, visit www.activeimplants.com.

CAUTION Investigational device. Limited by United States law to investigational use.

Contacts

Merryman Communications
Joni Ramirez, 323-532-0746
joni@merrymancommunications.com

Thomas Wickiewicz, MD, Inducted Into the AOSSM Hall of Fame

New York, NY—July 21, 2017

Thomas Wickiewicz, MD, sports medicine surgeon at Hospital for Special Surgery (HSS), was inducted today into The American Orthopaedic Society for Sports Medicine (AOSSM) Hall of Fame. This recognition is one of the highest honors given to an AOSSM member. Dr. Wickiewicz was presented with an award plaque during the AOSSM Annual Meeting in Toronto, Ontario.

“I am truly honored to be in the company of these extraordinary leaders in sports medicine,” said Dr. Wickiewicz. “I have focused my career on developing innovative minimally invasive surgical techniques designed to help patients get back to what they love doing most. For athletes of all levels, that is typically a return to sport.”

AOSSM Hall of Fame members are first nominated by their peers and then selected by the Hall of Fame committee. The Hall of Fame was established in 2001 to honor members of the orthopedic sports medicine community who have contributed significantly to the specialty. AOSSM is a world leader in sports medicine education, research, communication and fellowship, and includes national and international orthopaedic sports medicine leaders.

“Sports medicine is constantly evolving over the years as our research continues to advance the field,” said Dr. Wickiewicz. “Being a surgeon means being a student for the rest of your life. Education is critical to maintaining a robust medical practice over time.”

Dr. Wickiewicz joins fellow HSS sports medicine surgeon Russell F. Warren, MD, in the Hall.

 

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Invibio and Carbofix Partnering With UK Olympic Sprinter James Ellington on New “Passion For Progress” Initiative

THORNTON CLEVELEYS, EnglandJuly 13, 2017 /PRNewswire/ —

UK Olympic sprinter James Ellington has joined forces with the UK´s Invibio Biomaterial Solutions and CarboFix Orthopedics on his road to recovery and his overall ambition to return to the world stage of athletic competition after a devastating motorcycle accident in Tenerife earlier this year.

(Photo: http://mma.prnewswire.com/media/535235/Invibio_Biomaterial_Solutions.jpg )

The two companies and the athlete share a passion for progress and pushing boundaries; for James Ellington, mentally and physically first in sport and now in recovery, and for CarboFix and Invibio with innovative biomaterials and devices that have the potential to change the treatment of trauma fractures. For patients recovering from traumatic injuries this could serve as an inspiration not to lose track of their goals and passion.

Changes in destiny couldn´t be more pronounced for an athlete like James Ellington, who suddenly turned from being a world-class, elite sprinter training for his next competition to a patient in recovery facing an unknown future. However, even the life-changing experience of a severe head-on collision of his motorbike with a car hasn’t stopped James Ellington from fighting for his goals, despite having his legs and pelvis completely smashed.

“In extreme situations, it’s important not to lose faith and to consider all (therapeutic) options available,” explains Ellington. “I had a severe tibia fracture, and was offered two choices to fix it: a traditional Titanium nail or a Carbofix nail using a relatively new, but promising carbon fibre, composite technology. For me, it’s all about giving myself the best chance of achieving my goal and returning to competitive athletics. I chose the Carbofix nail because it’s lighter weight and for its faster healing potential.” Continues Ellington, “The rod is made from a new composite polymer. It’s strong, in a way that’s similar to metal implants, but not as stiff, which means it has the capability to stress the bone more and provide some micro-motion, so it works more like natural bone. The idea is that this will help support a quicker recovery – which is what convinced me this was the right path for me.” The sprinter nevertheless considers himself lucky: because he survived, is not paralyzed, is walking again and is so far on a good recovery path that may also include running in the future.

With trauma implants made from Invibio’s PEEK-OPTIMA™ Ultra-Reinforced, a composite polymer, CarboFix Orthopedics is hoping to support James and other patients in a similar position. Ron Szekely, the company´s Vice President of Sales and Marketing, says: “The aim itself to get back on track is fantastic, whether that’s the athletic track or returning to other individual recovery goals. This can be an important driver for rehabilitation. In addition to dedication and enthusiasm, patients need to have access to innovative medical devices that can support this. At CarboFix we believe in the potential of changing trauma treatment to improve the quality of life for many patients.”

Coming back (on track): high quality of life is an important aspect for recovery

“James Ellington´s passion for progress is the common denominator and connecting link between himself and Invibio,” explains Medical Business Unit Director, John Devine of Invibio Biomaterial Solutions. “Metals have been used to treat trauma fractures for decades, but patient demands for a quicker recovery with fewer device breakages coupled with the global increase in patient risk factors such as obesity and diabetes mean we need to be open to progress. That includes being open to the possibility that new innovative carbon fibre reinforced devices made from less stiff materials could really change how successful surgery and patient recovery is. The medical (device) industry itself very often and for good reasons, has to make small albeit important steps, to overcome challenges and achieve substantial progress towards the ultimate objective of improving patient outcomes and quality of life. James knows exactly how that feels and his positive attitude and firm belief in capabilities and future performance is another point we have in common.”

Inspiring people to achieve new records

This “passion for progress” after a traumatic injury or challenging operation is a theme supported by the two companies and centering on James Ellington´s hope to become an active athlete again. Together, Ellington, CarboFix and Invibio are pleased that James has already achieved so much in the months since the accident. The progress and hope shown by James Ellington could also help and inspire patients and trauma surgeons alike – whether Ellington is a pioneer by being an Olympic athlete sprinter again, or simply back and participating in the race of life.

About CarboFix

CarboFix Orthopedics, is the world-wide leader in developing, manufacturing and marketing orthopedic implants made of continuous Carbon-Fiber reinforced polymers.

The products company currently markets around the world its Piccolo Trauma and Carboclear spine lines.

CarboFix is working worldwide through its distributor network and through its subsidiaries in the US, China and Israel.
https://www.carbo-fix.com/

About Invibio Biomaterial Solutions
Invibio, a Victrex plc company, is a global leader in providing high performance biomaterial solutions to medical device manufacturers.  The company provides PEEK-OPTIMA™ polymers, advanced technical research and support and manufacturing of components for spine, trauma and orthopedic medical segments for the development of long implantable medical devices. Today, Invibio’s PEEK-OPTIMA™ polymers are used in around nine million implanted devices worldwide.

INVIBIO™, PEEK-OPTIMA™, INVIBIO BIOMATERIAL SOLUTIONS™ are trademarks of Victrex plc or its group companies.  All rights reserved.

About Victrex plc

Victrex, headquartered in the UK, is an innovative world leader in high performance polymer solutions focused on the Aerospace, Automotive, Electronics, Energy and Medical markets. Every day, millions of people rely on products or applications which contain our polymers, from smartphones, aeroplanes and cars to oil & gas operations and medical devices. With over 35 years’ experience, we are delivering leading edge solutions to shape future performance for our customers and our markets, and to drive value for our shareholders. Find out more at http://www.victrexplc.com

Copyright ©2017 Invibio Ltd.

SOURCE Invibio Biomaterial Solutions

Smith & Nephew joins forces with Imperial’s Biomechanics Group

19 July 2017/by Naomi Black

The medical device giant Smith & Nephew have signed a 3-year partnership with a research group in the Department of Mechanical Engineering to find new ways to support one of our most important joints.

With an increasing participation in sport, and a trend to keep active later in life, the treatment of sports injuries of the knee has been identified by Smith & Nephew as one offering high growth opportunities.

The USD $1m research study is led by Professor Andrew Amis, Professor of Orthopaedic Biomechanics and leader of The Biomechanics Group, who already has a long-standing working relationship with the company.  His expertise with artificial ligaments and total and partial knee prostheses as well as field experience working directly with surgeons has set the groundwork for this latest agreement.

 

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DJO Global Named Official Sports Brace of U.S. LaCrosse

Paul Ohanian / June 26, 2017

US Lacrosse announced today that DJO Global has been named as the Official Sports Brace of US Lacrosse and Supporting Partner of Team USA.

DJO Global, Inc. is a medical device company that produces a variety of orthopedic products for rehabilitation, pain management and physical therapy, and provides advanced protective and preventive technologies to the world’s most elite athletes.

As part of the partnership, Team USA players will wear DJO Global brand bracing and durable goods products exclusively, and receive medical treatments through the use of state-of-the art equipment.

Collaboration on injury prevention research will also be among the priorities of the partnership.

“This is a great opportunity for our Center for Sport Science to work with a world leader in sports medicine while also providing a valuable benefit to all of our members,” said Dr. Bruce Griffin, director of the Center for Sport Science at US Lacrosse.

 

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Vericel to Host Symposium on MACI Implant for Treating Articular Cartilage Defects in the Knee at AOSSM 2017 Annual Meeting

CAMBRIDGE, Mass., July 13, 2017 (GLOBE NEWSWIRE) — Vericel Corporation (NASDAQ:VCEL), a leading developer of expanded autologous cell therapies for the treatment of patients with serious diseases and conditions, announced today that the company is hosting a symposium on the  MACI® (autologous cultured chondrocytes on porcine collagen membrane) implant for treating articular cartilage defects in the knee at the American Orthopedic Society for Sports Medicine’s 2017 Annual Meeting.

Symposium topics will include a review of MACI published clinical studies, patient case profiles, and a discussion of the regulatory approval process for MACI.  Featured speakers include Daniël Saris, MD, PhD, Professor of Orthopedics at University Medical Center in Utrecht, Netherlands; Alison Toth, MD, Associate Professor of Orthopaedic Surgery at Duke University in Durham, North Carolina; Eric Strauss, MD, Assistant Professor of Orthopaedic Surgery at the NYU Hospital for Joint Diseases in New York; Seth Sherman, MD, Assistant Professor of Orthopaedic Surgery at the University of Missouri in Columbia; and David Recker, MD, Vericel’s chief medical officer.

The symposium, entitled  “The MACI Implant for Treating Articular Cartilage Defects in the Knee,” is being held on Thursday, July 20, 2017 from 12:30 – 2:00 pm at the Metro Toronto Convention Center, 700 Level, Room 205.

To register for the symposium and for more information, go to:  http://BIT.LY/AOSSM-MACI

Editor’s Note:
Vericel will have MACI information at Booth #619 at the AOSSM 2017 Annual Meeting.

About MACI
MACI® (autologous cultured chondrocytes on porcine collagen membrane) is an autologous cellular scaffold product that is indicated for the repair of symptomatic single or multiple full-thickness cartilage defects of the knee with or without bone involvement in adults.  The MACI implant consists of autologous cultured chondrocytes seeded onto a resorbable Type I/III collagen membrane.  Autologous cultured chondrocytes are human-derived cells which are obtained from the patient’s own cartilage for the manufacture of MACI.

Important Safety Information

  • MACI is contraindicated in patients with a known history of hypersensitivity to gentamicin, other aminoglycosides, or products of porcine or bovine origin.  MACI is also contraindicated for patients with severe osteoarthritis of the knee, inflammatory arthritis, inflammatory joint disease, or uncorrected congenital blood coagulation disorders.  MACI is also not indicated for use in patients who have undergone prior knee surgery in the past six months, excluding surgery to procure a biopsy or a concomitant procedure to prepare the knee for a MACI implant.
  • MACI is contraindicated in patients who are unable to follow a physician-prescribed post-surgical rehabilitation program. The safety of MACI in patients with malignancy in the area of cartilage biopsy or implant is unknown.  Expansion of present malignant or dysplastic cells during the culturing process or implantation is possible.
  • Patients undergoing procedures associated with MACI are not routinely tested for transmissible infectious diseases.  A cartilage biopsy and MACI implant may carry the risk of transmitting infectious diseases to healthcare providers handling the tissue.  Universal precautions should be employed when handling the biopsy samples and the MACI product.

About Articular Cartilage Defects of the Knee
Articular cartilage is a highly organized avascular tissue composed of chondrocytes embedded within an extracellular matrix of collagens, proteoglycans and noncollagenous proteins.  Its primary function is to enable the smooth articulation of joint surfaces, and to cushion compressive, tensile and shearing forces.  Articular cartilage damage is caused by both acute and repetitive trauma resulting in knee pain, effusion or mechanical symptoms such as catching and locking, and swelling.  Since articular cartilage is avascular it has little capacity to repair itself or regenerate.  Articular cartilage lesions that are left untreated may progress to debilitating joint pain, dysfunction, and osteoarthritis.1  The prevalence rate for cartilage lesions in the knee has been reported to be 63% in patients undergoing investigational arthroscopies.2

About Vericel Corporation
Vericel develops, manufactures, and markets autologous expanded cell therapies for the treatment of patients with serious diseases and conditions. The company markets two cell therapy products in the United States. Vericel is marketing MACI® (autologous cultured chondrocytes on porcine collagen membrane), an autologous cellularized scaffold product indicated for the repair of symptomatic, single or multiple full-thickness cartilage defects of the knee with or without bone involvement in adults. Carticel® (autologous cultured chondrocytes) is an autologous chondrocyte implant for the treatment of cartilage defects in the knee in patients who have had an inadequate response to a prior arthroscopic or other surgical repair procedure. Vericel is also marketing Epicel® (cultured epidermal autografts), a permanent skin replacement for the treatment of patients with deep dermal or full thickness burns greater than or equal to 30% of total body surface area. Vericel is developing ixmyelocel-T, an autologous multicellular therapy intended to treat advanced heart failure due to ischemic dilated cardiomyopathy. For more information, please visit the company’s website at www.vcel.com.

Epicel®, Carticel®, and MACI® are registered trademarks of Vericel Corporation. © 2017 Vericel Corporation. All rights reserved.

This document contains forward-looking statements, including, without limitation, statements concerning anticipated progress, objectives and expectations regarding the commercial potential of Vericel products, intended product development, clinical activity timing, regulatory process, and objectives and expectations regarding our company described herein, all of which involve certain risks and uncertainties. These statements are often, but are not always, made through the use of words or phrases such as “anticipates,” “intends,” “estimates,” “plans,” “expects,” “we believe,” “we intend,” and similar words or phrases, or future or conditional verbs such as “will,” “would,” “should,” “potential,” “can continue,” “could,” “may,” or similar expressions. Actual results may differ significantly from the expectations contained in the forward-looking statements. Among the factors that may result in differences are the inherent uncertainties associated with competitive developments, clinical trial and product development activities, regulatory approval requirements, estimating the commercial potential of our products and product candidates, market demand for our products, product performance, ability of ICT to obtain approval to transfer funds to the U.S., and our ability to supply or meet customer demand for our products. These and other significant factors are discussed in greater detail in Vericel’s Annual Report on Form 10-K for the year ended December 31, 2016, filed with the Securities and Exchange Commission (“SEC”) on March 13, 2017, Quarterly Reports on Form 10-Q and other filings with the SEC. These forward-looking statements reflect management’s current views and Vericel does not undertake to update any of these forward-looking statements to reflect a change in its views or events or circumstances that occur after the date of this release except as required by law.

References

1Bedi A, Feeley BT, Williams RJ. Management of articular cartilage defects of the knee. J Bone Joint Surg Am. 2010;92(4):994‑1009.

2Curl WW, Krome J, Gordon ES, Rushing J, Smith BP, Poehling GG. Cartilage injuries: a review of 31,516 knee arthroscopies. Arthroscopy. 1997;13(4):456-60.

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Active Implants Appoints Charles W. Federico and Gary D. Henley to Board

July 12, 2017

MEMPHIS, Tenn.–(BUSINESS WIRE)–Active Implants, a company that develops orthopedic implant solutions, today announced the appointments of orthopedic and sports medicine industry veterans Charles W. Federico and Gary D. Henley to its board of managers.

“Both Charlie and Gary are respected leaders with long-term success in medical and orthopedic device industries, and they bring a wealth of strategic and operational experience to our board,” said Ted Davis, president and chief executive officer of Active Implants. “We believe their diverse leadership experience will strengthen our board, and their insights will be invaluable as we continue to develop the NUsurface Meniscus Implant and fulfill a significant unmet need in the orthopedic market here in the U.S. and worldwide.”

Federico has 44 years of experience in the medical device industry, with significant focus in the sports medicine segment while president and chief executive officer of Orthofix International N.V. and president of Smith & Nephew Endoscopy. Additionally, he has held senior management and sales and marketing positions with Dyonics, General Foods Air Products Corporation, Puritan Bennett Corporation and LSE Corporation. Federico has extensive board experience, including chairman of the board and lead director of MAKO Surgical Corp, sold to Stryker; and a board member at Biomimetic Therapeutics, sold to Wright Medical Group.

Henley has more than 35 years of experience in the orthopedic device industry, including president, chief executive officer and board member of United Orthopedic Group, which was sold to Breg. Previously, he was president and chief executive officer of Wright Medical Group, Inc.; president of Orthofix International N.V.’s Americas Division; president of Smith & Nephew’s Endoscopy Video Division; and president and chief executive officer of Cecorp, Inc. Henley is an experienced board member and industry consultant, most recently serving as executive chairman of the board of directors at OrthAlign, Inc. and a director at Orchid Orthopedic Solutions.

With the appointment of Federico and Henley, Active Implants’ board consists of eight members: Henry Klyce, chairman of the board; Ted Davis, Active Implants CEO; James D. Lackie; William T. Mays, Jr.; Haynes Morris; and Spence Wilson, Jr.

About the NUsurface® Meniscus Implant

The NUsurface® Meniscus Implant is an investigational treatment for patients with persistent knee pain following medial meniscus surgery. It is made from medical grade polymer and, as a result of its unique materials, composite structure and design, does not require fixation to bone or soft tissues. The NUsurface Meniscus Implant mimics the function of the natural meniscus and redistributes loads transmitted across the knee joint. The NUsurface Meniscus Implant has been used in Europe under CE Mark since 2008 and in Israel since 2011. Clinical trials are underway in the U.S., Europe and Israel to verify the safety and effectiveness of the NUsurface Meniscus Implant.

About Active Implants LLC

Active Implants LLC develops orthopedic implant solutions that complement the natural biomechanics of the musculoskeletal system, allowing patients to maintain or return to an active lifestyle. Active Implants is privately held with headquarters in Memphis, Tennessee. European offices are in Haarlem, The Netherlands, with R&D facilities in Netanya, Israel. For more information, visit www.activeimplants.com.

CAUTION Investigational device. Limited by United States law to investigational use.

Contacts

Merryman Communications
Joni Ramirez, 323-532-0746
joni@merrymancommunications.com

TOCA (The Orthopedic Clinic Association) Performs First Meniscus Replacements in Arizona with NUsurface® Meniscus Implant

July 06, 2017

PHOENIX–(BUSINESS WIRE)–TOCA (The Orthopedic Clinic Association), a one-stop resource for orthopedics in Arizona, and Active Implants, a company that develops orthopedic implant solutions, today announced that the first meniscus replacement procedures in Arizona were successfully performed by Dr. Tom Carter. TOCA is the only center in the state – and one of just 10 sites nationwide – enrolling patients with persistent knee pain caused by injured or deteriorating meniscus cartilage in the SUN trial, which is designed to assess the safety and effectiveness of the NUsurface® Meniscus Implant (pronounced “new surface”) in restoring function similar to that of a natural, healthy meniscus.

One of the first patients to receive the implant in Arizona was Robert Nowlan, a 55-year-old Anthem resident, who first tore his meniscus 17 years ago while hiking in the Grand Canyon. Although he underwent three surgeries and injection therapy to treat the injury, he experienced constant pain that limited his daily activity. Nowlan’s knee was consistently throbbing with pain whether he was walking, working or even sitting. The pain became so intense, he had to give up hobbies he loved like running, hiking and karate.

The meniscus is a tissue pad between the thigh and shin bones. Once damaged, the meniscus has a very limited ability to heal. Over 1 million partial meniscectomies to remove or repair a torn meniscus are performed in the U.S. every year, about the same as the total number of hip and knee replacement surgeries combined. However, many patients still experience persistent knee pain following meniscus surgery.

“There aren’t many options for patients who experience persistent knee pain following meniscus surgery,” said Dr. Tom Carter, orthopedic surgeon at TOCA. “We hope the NUsurface implant decreases or alleviates pain in these patients, helps them delay knee replacement surgery, and improves their level of activities.”

Nowlan received the NUsurface Meniscus Implant in October 2016 through a small incision in his knee and completed a six-week rehabilitation program. Eight months into his recovery, he is most looking forward to biking and hiking the Grand Canyon again with his family – but this time pain-free.

“My knee pain over the last 17 years had reduced my quality of life, as I was too young for knee replacement and had resigned myself to just living and working with constant pain,” Nowlan said. “A couple weeks after receiving the NUsurface Meniscus Implant, the knee pain I was used to living with was gone. It felt like I drank from the fountain of youth – I can finally walk around and do all the activities I’ve been missing out on.”

The NUsurface Meniscus Implant has been used in Europe under CE Mark since 2008 and Israel since 2011.

About the Clinical Trial

The SUN study (Safety Using NUsurface®) will enroll approximately 120 patients as part of regulatory process to gain approval from FDA to sell the device in the U.S. All patients who meet study requirements and agree to enter the trial are offered the NUsurface Meniscus Implant as treatment. Treatment with NUsurface in the SUN trial is eligible for coverage by Medicare and some private insurance companies. To be eligible for the study, participants must be between the ages of 30 and 75 and have pain after medial meniscus surgery that was performed at least six months ago. To learn more about the SUN study, please visit http://sun-trial.com or call (844) 680-8951.

About the NUsurface® Meniscus Implant

The NUsurface® Meniscus Implant is an investigational treatment for patients with persistent knee pain following medial meniscus surgery. It is made from medical grade plastic and, as a result of its unique materials, composite structure and design, does not require fixation to bone or soft tissues. The NUsurface Meniscus Implant mimics the function of the natural meniscus and redistributes loads transmitted across the knee joint. Clinical trials are underway in the U.S., Europe and Israel to verify the safety and effectiveness of the NUsurface Meniscus Implant.

About TOCA (The Orthopedic Clinic Association)

TOCA (The Orthopedic Clinic Association) has served the Valley with orthopedic care since it was founded in 1949. TOCA is a one-stop resource for orthopedics in Arizona, led by nationally recognized, established orthopedic physicians who are passionate about quality care. TOCA brings expertise in orthopedics and sports medicine, numerous sub-specialties, physical therapy and hand therapy. Each TOCA Physician brings their own passion and integrity to a common purpose, honoring TOCA’s mission statement: “Serving our Patients through Innovative and Comprehensive Orthopedic Care.” Our physicians and staff are dedicated to providing for each person’s needs and ensuring the highest level of care for a wide range of musculoskeletal conditions. For more information, visit http://tocamd.com/.

About Active Implants

Active Implants, LLC develops orthopedic implant solutions that complement the natural biomechanics of the musculoskeletal system, allowing patients to maintain or return to an active lifestyle. Active Implants is privately held with headquarters in Memphis, Tennessee. European offices are in Driebergen, The Netherlands, with R&D facilities in Netanya, Israel. For more information, visit www.activeimplants.com.

CAUTION Investigational device. Limited by United States law to investigational use.

Contacts

Active Implants, LLC
Merryman Communications
Joni Ramirez, 323-532-0746
joni@merrymancommunications.com
or
TOCA
Lisa Paulson, 602-512-8525
lpaulson@tocamd.com