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Vertebral fixation (also known as "spinal fixation") is an orthopedic surgical procedure in which two or more vertebrae are anchored to each other through a synthetic "vertebral fixation device", with the aim of reducing vertebral mobility and thus avoiding possible damage to the spinal cord and/or spinal roots.
Beryllium-aluminum alloy an alloy that consists of 62% beryllium and 38% aluminum, by weight, corresponding approximately to an empirical formula of Al 2 Be. It was first developed in the 1960s by the Lockheed Missiles and Space Company, who called it Lockalloy, [1] [2] and used as a structural metal in the aerospace industry because of its high specific strength [3] and stiffness. [4]
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Ti-6Al-4V (UNS designation R56400), also sometimes called TC4, Ti64, [1] or ASTM Grade 5, is an alpha-beta titanium alloy with a high specific strength and excellent corrosion resistance.
Portable Document Format (PDF), standardized as ISO 32000, is a file format developed by Adobe in 1992 to present documents, including text formatting and images, in a manner independent of application software, hardware, and operating systems.
computational simulations of acetabular hip component to assist with total hip replacement surgery in a collaboration with University of Pittsburgh Medical Center; development of medial surface algorithms in collaboration with Sandia National Laboratories. Awards. Fellow of American Society of Mechanical Engineers (ASME).
One can find titanium in neurosurgery, bone conduction hearing aids, false eye implants, spinal fusion cages, pacemakers, toe implants, and shoulder/elbow/hip/knee replacements along with many more. The main reason why titanium is often used in the body is due to titanium's biocompatibility and, with surface modifications, bioactive surface.
Medical Device Alert: DePuy ASR TM acetabular cups used in hip resurfacing arthroplasty and total hip replacement, Medicines and Healthcare products Regulatory Agency, MDA/2010/044, 25 May 2010; Medical Device Alert: All metal-on-metal (MoM) hip replacements, Medicines and Healthcare products Regulatory Agency, MDA/2012/008, 28 February 2012