SI-BONE, Inc. Announces Publication of Postmarket Surveillance Safety Data on First 5,319 Patients Treated with iFuse Implant SystemJune 5, 2013 7:00 am | by The Associated Press | News | Comments
SI-BONE, Inc. (San Jose, California), a medical device company that is pioneering the use of a minimally invasive surgical (MIS) device to fuse the sacroiliac (SI) joint, announced today the publication of the iFuse Implant System's@ postmarket surveillance safety data for the first 5,319 patients treated.
Blue Belt Technologies, Inc., an innovative medical technology company commercializing robotic-assisted solutions for orthopedic surgery, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its STRIDE™ Unicondylar Knee implant system.
Providence Medical Technology, Inc. (PMT) today announced it received 510(k) clearance from the FDA for its PMT Cervical Cage. PMT Cervical Cage is a novel minimally-invasive implant and delivery system for cervical fusion procedures. PMT Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level.
The growth in sales of medical technologies is set to outperform prescription medicines over the coming five years. Data from Evaluate Medtech indicates that over the period 2011 to 2018, the overall global compound annual growth rate for the sector will be 4.4%, in contrast to just 2.5% for drug products.
Scientists have taken a vital step forward in understanding how cells from skin tissue can be reprogrammed to become stem cells. New research could pave the way to generate these stem cells efficiently to better understand and develop treatments for diseases such as multiple sclerosis, Parkinson's disease, and muscular degeneration.
Ceramic materials have been used for artificial joints since the 1970s, yet the need for smaller medical implants with more complicated structures has created exciting new opportunities for those manufacturing ceramic solutions for the medical market. As a result, detailed and complex ceramic components are becoming increasingly specified for a wide range of applications.
The Food and Drug Administration today granted 510(k) clearance to a muscle and joint rehabilitation medical device developed by OHSU Scientist Dr. Paul Cordo, Ph.D., and AMES Technology, Inc. AMES is an Oregon Health & Science University spinoff company established to transform Dr. Cordo's OHSU research findings into a rehabilitation medical device for use in hospitals and clinics.
NuVasive, Inc., a medical device company focused on developing minimally disruptive surgical products and procedures for the spine, is excited to announce the global launch of its Maximum Access Surgery Posterior Lumbar Interbody Fusion (MAS® PLIF) procedure.
NJIT Distinguished Professor and electrical engineer Atam Dhawan hits the lecture trail again this summer as a distinguished speaker for an IEEE life sciences lecture series. His focus will be how "Point of Care Healthcare" can reduce illness, improve the quality of life, and stop spiraling healthcare costs. Dhawan, who will stop at conferences in Japan, Colombia and Croatia, tells audiences about the following.
The technology at the heart of the next generation of medical devices is critical to our ability to offer comprehensive care in the coming decades. While our current systems of care have served us well thus far, they are crumbling under the pressures of modern expectations of care, economics, scale, and the sheer breadth of medical science.
AUDUBON, Pa.--(BUSINESS WIRE)--May 23, 2013--Algea Therapies, a division of Globus Medical Inc. (NYSE: GMED), committed to finding innovative, minimally invasive solutions that treat pain and restore quality of life, today announced the launch of the SHIELD™ Vertebral Compression Fracture (VCF)...
Surgical simulators are an ideal solution for training surgeons with minimal risk to patient health and safety. This is particularly important when surgeons train for procedures utilizing arthroscopy because it requires the surgeon to perform the surgery while looking at a camera screen instead of the patient. This necessitates extensive training to ensure the doctor is an expert in the method.
Eric Olson is the chief executive officer and president of Amedica, the only company that produces medical grade Silicon Nitride. He took a moment to participate in the following Q&A about the unique material and its impact in medical devices, specifically in the orthopedic implant area.
Stryker Corporation's Orthopaedics division and OrthoSensor, Inc., the leader in intelligent orthopedics, today announced an extension of their co-marketing agreement for Stryker's Triathlon Knee System and OrthoSensor's VERASENSE. VERASENSE is an intelligent instrument system that provides...
NEW YORK--(BUSINESS WIRE)--May 22, 2013--Wendy Fleishman of the national plaintiffs’ law firm Lieff Cabraser Heimann & Bernstein, LLP, announced that the firm issued today a list of answers to frequently asked questions (FAQ) from hip replacement patients who received the Stryker Rejuvenate or...
When Chinese exchange student Jiahone Guo suffered a cranial injury during a club soccer match, he thought "maybe I will go to see God," according to a report on WFAA-TV in Dallas/Fort Worth, Texas. Fortunately, due to timely surgery and a custom-made prosthetic skull plate designed by MedCAD, Guo is able to do almost everything he could do before the fateful match.
Physicians at Monash University and The Alfred Hospital in Melbourne, Australia describe the logistic, medical, and societal challenges faced in treating spine trauma in morbidly obese patients. The authors categorize difficulties faced in the care of morbidly obese patients from on-scene immobilization and medical transport through spinal imaging, surgery, and postoperative care.
Medical devices are any medical items that are neither a drug nor a biological product. In light of their different mechanisms, actions and regulatory requirements, medical device (MD) trail evaluations are much more complicated than drug trails due to their unique clinical practices....
Wright Medical Hip Lawsuit Update: New Video Informs Patients Why Profemur Z Hip Implant Is Allegedly FailingMay 17, 2013 1:41 pm | by The Associated Press | News | Comments
SAN FRANCISCO--(BUSINESS WIRE)--May 17, 2013--Kent Klaudt, an injury lawyer at the national plaintiffs’ law firm Lieff Cabraser Heimann & Bernstein, LLP, announced that Lieff Cabraser released today a video on the injuries suffered by hip replacement patients who received the Profemur Z hip...
PITTSBURGH--(BUSINESS WIRE)--May 17, 2013--Blue Belt Technologies, Inc., an innovative medical technology company commercializing robotic solutions for orthopedic surgery, announces an implant partnership with DJO Surgical, a DJO Global Company. Blue Belt’s NavioPFS orthopedic surgical system...
OrthoView Announces the U.S. Launch of a New, Subscription-based, Digital Planning and Templating Solution for Individual Orthopaedic SurgeonsMay 16, 2013 2:01 pm | by PR Newswire | News | Comments
JACKSONVILLE, Florida, May 16, 2013 /PRNewswire/ -- OrthoView PSL will allow individual surgeons in private practice in the U.S. to access the widely-used OrthoView digital templating software via the Cloud and requires just a PC and Internet connection to get started. OrthoView, the...
Legal-Bay LLC, the Lawsuit Settlement Funding Company, has issued an update on two major hip implant litigations in the mass tort market. And the results are completely different. Legal-Bay believes the Stryker hip litigation on the ABG II and the Rejuvenate which have been already recalled by the company will see a smoother road for plaintiffs looking for a settlement in the not so distant future.
At an event held at Hospital for Special Surgery, GE Healthcare introduced MAVRIC SL, a novel magnetic resonance imaging technique designed to address the growing clinical need to more accurately image soft tissue and bone in patients with MR Conditional-labeled implants, such as joint replacements and other instrumentation.
Knees can perform extraordinary tasks, but when all the activity they encounter takes too great a toll over time, total knee replacement surgery may be advisable. Product developers and manufacturers have to create total knee replacement implants that will perform as long as possible. Realistic simulation with finite element analysis software has now become vital to that process.
On average, implantable devices account for 30 percent of total hospital supply spend, and make up 50 to 80 percent of the total cost for some procedures. Despite these large numbers, processes around managing and tracking these devices are rife with inefficiencies and revenue leakage.