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FDA Device Info: Deidentified original patient data from the CARTIVA MOTION trial
FDA Device Info: Deidentified original patient data from the CARTIVA MOTION trial
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Deidentified original patient data from the CARTIVA MOTION trial (PMA number P150017).
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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