The U.S. Food and Drug Administration (FDA) is warning patients and healthcare providers of a “higher than expected risk” of failure in Stryker Scandinavian Total Ankle Replacement (STAR) devices.
Please provide your email address to receive an email when new articles are posted on . QUEBEC CITY — In this video from the American Orthopaedic Foot & Ankle Society Annual Meeting, Jensen K. Henry, ...
The FDA reminded healthcare providers and patients on Thursday that several Exactech joint replacement devices packaged in defective bags should be closely monitored for device wear or failure. Many ...
Ankle fusion and total joint replacement are the two main options for definitive treatment of advanced arthritis. This large British study found that revision rates were significantly higher with ...
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