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This month people can continue to focus on getting exercise or on their diet. Meanwhile, the best way to have a healthier heart is to consider how diet and movement work together to keep hearts healthier and reduce cardiovascular disease risks.
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Catalyst OrthoScience Inc. has announced U.S. Food and Drug Administration (FDA) 510(k) clearance of its Archer Patient-Specific Instrumentation (PSI).
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Cara Medical Ltd. recently announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the CARA System, a computed tomography angiography (CTA)-based platform that provides noninvasive, patient-specific three-dimensional (3D) visualization of the cardiac conduction system.
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The U.S. Food and Drug Administration (FDA) has cleared the new Xenocor Saberscope, a single-use 5mm articulating laparoscope designed for high-definition (HD) visualization during minimally invasive abdominal (belly) and thoracic (chest) surgical procedures.
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Olympus Corp. of the Americas has announced FDA clearance of the pediatric use indication for two single-use bronchoscopes in the respiratory portfolio distributed by Olympus.
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If you are an OR nurse committed to patient safety, this PDF breaks down a hidden but significant risk in minimally invasive surgery: insulation failure in electrosurgical instruments.
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For over 20 years, OR Today has provided perioperative and SPD professionals with up-to-date news and information about their profession. The magazine aims to educate readers about new guidelines, techniques, and equipment, as well as practical information for career building, problem-solving and overall well-being.
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