The KineSpring System is designed to be a first surgical option for patients with knee osteoarthritis (OA). It is intended to treat the symptoms of pain and loss of knee function secondary to OA of the medial compartment of the knee.
The lightweight skeletons of organisms such as sea sponges display a strength that far exceeds that of manmade products constructed from similar materials. Scientists have long suspected that the difference has to do with the hierarchical architecture of the biological materials...
A new ASTM International standard will provide a consistent method for analyzing hip stems used in hip replacement surgery. The new standard, ASTM F2996, Practice for Finite Element Analysis (FEA) of Nonmodular Metallic Orthopaedic Hip Femoral Stems, was developed by Subcommittee F04.22 on Arthroplasty, part of ASTM International Committee F04 on Medical and Surgical Materials and Devices.
Manny Villafaña, Chairman and Chief Executive Officer of Kips Bay Medical, Inc., a medical device company focused on manufacturing and commercializing its external saphenous vein support technology, eSVS® Mesh, for use in coronary artery bypass grafting surgery (CABG), provided the following business update to Kips Bay shareholders and the financial community.
For the 1st time Mazor Robotics' Renaissance robot-assisted surgical system system was used to to treat a Parkinson's patient, implanting a battery-sized neurostimulator that delivers mild electrical stimulation to targeted areas of the brain. The landmark procedure took place at a Florida hospital earlier this month.
A team of University of California, Riverside researchers have developed a novel transparent skull implant that literally provides a "window to the brain", which they hope will eventually open new treatment options for patients with life-threatening neurological disorders, such as brain cancer and traumatic brain injury.
A sales rep's visit could be worth as much as $230 per case in surgeons' use of coronary stents, according to a study in the American Heart Journal. The presence of a company sales rep in the cath lab increased the likelihood that surgeons would opt for drug-eluting over bare-metal stents, researchers said.
In a materials science laboratory at Harvard University, a transparent disk connected to a laptop fills the room with music—it's the "Morning" prelude from Peer Gynt, played on an ionic speaker. No ordinary speaker, it consists of a thin sheet of rubber sandwiched between two layers of a saltwater gel, and it's as clear as a window.
The U.S. Food and Drug Administration (FDA) hit Allendale, NJ-based Stryker’s Spine division with a Class I recall for the company’s OASYS Midline Occiput Plate. According to reports, Stryker learned that a post-operative fracture can occur in the pin that connects ...
While machining may not be specified as much as it once was in the medical device industry (outside of the orthopedic realm, that is), it is still very much a necessary component fabrication process for this industry. In fact, machining is being utilized across an array of device sectors, from surgical tools, fixation devices, and dental implants to components for medical pumps, instrumentation, and implantables.
While the use of disposables in healthcare is certainly nothing new, their implementation as instrumentation in orthopedic procedures is. Offering an array of benefits for OEMs and hospitals alike, such as cost savings, improved efficiencies, and enhanced safety, without sacrificing the durability and strength of more traditional instruments, it’s no wonder this trend is occurring.
Researchers at Missouri University of Science and Technology have developed a type of glass implant that could one day be used to repair injured bones in the arms, legs and other areas of the body that are most subject to the stresses of weight. This marks the first time researchers have shown a glass implant strong enough to bear weight can also integrate with bone and promote bone growth.
Biomet will go to bat over its M2A-magnum metal-on-metal hip implants after failing to convince an Indiana federal judge that a personal injury lawsuit was preempted by FDA rules. The plaintiff, Leslie Caccia, sued Biomet for a supposedly defective metal-on-metal hip implant in what is now part of a larger multi-district litigation.
The Vivistim System has been developed to treat stroke patients that experience an upper-limb deficit following their stroke. These are patients that are unable to fully recover the use of their upper-limbs at least 6 months following their stroke. A United Kingdom based clinical trial is underway using the Vivistim System in the Glasgow and Newcastle areas.
LDR, a privately held medical device company offering exclusive spinal implant technologies for both non-fusion and fusion applications, today announced that it has received a letter of approval from the U.S. Food and Drug Administration (FDA) allowing the commercial sale and distribution of the Mobi-C Cervical Disc (Mobi-C) for two-level indications...
Lombard Medical Technologies PLC, the specialist medical technology company focused on innovative vascular products, today announces that the first U.S. patients have been successfully treated with Aorfix, the Group’s flexible stent graft for the endovascular repair of abdominal aortic aneurysms.
Based on its recent analysis of the medical implantable textile structures design market, Frost & Sullivan recognizes Secant Medical, Inc. with the 2012 North American Frost & Sullivan Award for Enabling Technology. Combining variability in structure, delivery method, performance, physical composition, resorbability, and other unique elements that make up implantable textile constructions...
A 10-year-old Pennsylvania girl recovering from two double lung transplants is expected to be released from the hospital this week, a spokeswoman for the girl's family said Monday. Tracy Simon said a final decision hasn't been made on exactly when Sarah Murnaghan will leave Children's Hospital of Philadelphia.
Kent L. Klaudt, lawyer at the national plaintiffs’ law firm Lieff Cabraser Heimann & Bernstein, LLP, announced that U.S. District Court Judge G. Murray Snow of the District of Arizona denied in large part Medtronic’s motion to dismiss a personal injury lawsuit brought by Dr. Cristina Ramirez against the company on grounds that the claims are preempted by Federal law.
AngioDynamics has announced that the U.S. Food and Drug Administration has granted 510(k) clearance to Navilyst Medical Inc., an AngioDynamics company, for its BioFlo Port with Endexo technology designed to reduce the accumulation of catheter-related thrombus on, and in, the port catheter.
On this episode of The Pulse, brought to you by MDT TV, we are regenerating limbs, building better brain implants, engineering 3D tissue, and measuring consciousness.
C.R. Bard settled the 2nd bellwether trial over its Avaulta pelvic mesh just before it was supposed to go to trial, a week after losing a $2 million judgment in the 1st trial. Murray Hill, N.J.-based Bard and plaintiff Wanda Queen agreed to settle the case on undisclosed terms...
In early human tests, SetPoint Medical has found that an electronic implant helped reduce the symptoms of rheumatoid arthritis in six of eight patients. The company is one of many groups exploring the potential of electronic implants to treat diseases by delivering pulses to nerves that regulate organ or body functions.
Many women who have received a transvaginal mesh or sling implant have experienced serious health complications after surgery. The Food and Drug Administration has issued safety warnings concerning the health risks associated with these devices, which have been implanted in thousands of women for the treatment of conditions that result in weakened pelvic floor muscles...
House Research Institute (HRI) and Children’s Hospital Los Angeles announced today final approval of grant funding by the National Institutes of Health (NIH) National Institute on Deafness and Communications Disorders (NIDCD) for a major five-year, FDA-approved clinical trial of the auditory brainstem implant (ABI) in children.