![]() Additionally, it has been estimated that Infuse was used in over 100,000 spinal fusion surgeries on an annual basis from 2002 to 2013. Onze missie inspireert ons tot buitengewone oplossingen en ondersteuning die echt een positieve wending kunnen geven aan het leven van mensen. In September 2008, Medtronic reported that approximately 680,000 units of Infuse Bone Graft had been used in the United States. This cylinder is where the genetically engineered material called. From 2004 to 2008, the FDA received more than 40 reports of complications stemming from the Infuse device. The Infuse Bone Graft uses the LT-Cage Device which consists of a small hollow metal cylinder. In 2008, the FDA issued Medtronic a warning after receiving multiple reports of complications surrounding the Infuse Bone Graft. The Infuse Bone Graft lawsuits allege that Medtronic downplayed or failed to notify doctors of the risks associated with the bone protein and illegally marketed Infuse for unapproved off-label uses. It was given relatively limited approval in that it was authorized by the FDA only for use in single-level, lower-lumbar spinal fusions in which an anterior (through the stomach) surgical approach is used. Food and Drug Administration (FDA) approved Infuse in 2002. When combined with a collagen sponge and place inside a cage (fusion device), the bone graft is implanted into the spine and is supposed to eliminate the need for additional surgery. The Medtronic Infuse Bone Graft is used during surgery to stimulate bone growth and replace damaged spinal disks. Infuse rhBMP-2 is a “bone morphogenetic protein,” which is a genetically engineered version of a human protein designed to promote bone growth. ![]() after the Infuse Bone Graft was linked to serious side effects, including nerve damage, excessive bone growth and paralysis. If you or a loved one has undergone spinal fusion surgery using Medtronic Infuse BMP-2 and experienced problems, you may be eligible to file a Medtronic Infuse lawsuit.Īcross the country, patients are filing lawsuits against Medtronic Inc. are representing clients throughout California and nationwide who allege that they were severely injured by Medtronic’s Infuse Bone Graft. The skilled defective medical device lawyers at Cutter Law P.C.
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