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Devicemakers using material from animals that could carry transmissible spongiform encephalopathies should document the absence of TSE disease and standard vaccinations, such as live modified viruses, that the animal received, an updated FDA guidance says. Read More
The FDA granted AtheroMed’s Phoenix Atherectomy System 510(k) clearance to treat vessels below the knee in patients with peripheral artery disease. Read More
Stryker is bullish on robotic surgery, planning a first-half 2014 trial of its recently acquired Mako robotic surgery platform for use in full-knee replacements. Read More