![]() The types of harm and complications a patient can suffer from the non-approved use of the Infuse Bone Graft include ectopic or uncontrolled bone growth at or near the site of surgery. Examples of off-label uses include lumbar spine surgeries performed through a lateral approach (through the side of the body) or a posterior approach (through the back of the body). Yes, the Infuse Bone Graft is and has been used for non-approved uses to harvest bone growth. In 2002 the FDA approved the use of Infuse Bone Graft for an anterior approach lumbar fusion of one level of the spine between the L5 and S1 vertebrae. Yes, the Infuse Bone Graft is approved for one type of spinal surgery. Did the FDA approve the Infuse Bone Graft?.The main uses of the system are to create an alternative for bone growth. who is also the largest manufacturer of medical devices. ![]() The company that manufactures and sells the device is Medtronic Inc. This cylinder is where the genetically engineered material called rhBMP-2 (recombinant human Bone Morphogenetic Protein-2) is placed to stimulate human bone growth. The Infuse Bone Graft uses the LT-Cage Device which consists of a small hollow metal cylinder. What is the length of time the lawsuit will take to complete?.Are there any fees or cost for you to review my case?.When is the best time for me to hire legal counsel?.What will be the recovery I would receive?.If I do have a claim against Medtronic, what are the types of claims available to me?.Should patients hold the surgeon responsible for any injuries suffered or only Medtronic?.Should Medtronic be held responsible for the injuries suffered by individuals from the implant of the Infuse Bone Graft?. ![]()
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