Zimmer Biomet Holdings, Inc. announced today that it has received US Food and Drug Administration 510(k) clearance for its Rosa hip system for robotically assisted direct anterior total hip replacement, following the agency’s nod for the Rosa partial knee system in April.
This latest addition marks the fourth robotic system for the Rosa platform, including Rosa knee for total knee arthroplasty and Rosa One for neurosurgical and spine procedures, which is expected...
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