The US Food and Drug Administration (FDA) has expanded Titan Spine’s ENDOSKELTON® TA Vertebral Body Replacement Device (VBR) 510k to include an Interbody Fusion Device indication. Under its expanded 510K indication, the Endoskeleton® TA Interbody Fusion Device is approved for use in skeletally mature patients with Degenerative Disc Disease (DDD) at one or two contiguous levels from L2-S1.
A swallowed string may someday replace the invasive, uncomfortable endoscope now used to diagnose a devastating childhood disease of the esophagus. Steven J. Ackerman of University of Illinois at Chicago College of Medicine and Dr. Glenn T.
As the point-of-care for drug therapy shifts from the clinic to the home, drug developers are learning the importance of design integration, ergonomics, and concurrent engineering. Welcome to the age of combination products, an age where the drug is one part of a therapeutic product designed to meet the needs of a specific therapy or patient group. Recognizing the growing impact of combination products, the U.S.
In light of the aging population, the escalating cost impact of diseases common in the elderly on a country’s health care budget is of increasing importance. A country-specific evaluation of the costs associated with this condition is important for both clinicians and health care planners.
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The author discusses the case of Coombes v. Florio, in which the Massachusetts Supreme Judicial Court overturned a trial judge’s ruling to dismiss a lawsuit against a physician whose patient was the driver in a car accident that resulted in the death of a child. The trial judge had ruled that physicians’ responsibilities were restricted to their patients, whereas the court ruled that the victim of a car accident can sue the driver’s physician if the physician has failed to inform the patient about medication side effects that may impair driving.