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Patient registries are contributing significant data on the safety and effectiveness of implanted devices, and with the advent of the FDA’s unique device identification system, it is now possible to link implant characteristics to the Global UDI Database, a recent study suggests. Read More
The U.S. Food and Drug Administration plans to tighten restrictions on dozens of spinal screws already on the market, requiring new PMAs for dynamic stabilization systems that are used to treat severe spondylolisthesis, fracture, dislocation, scoliosis and spinal tumors. Read More