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Nuvectra

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead recall (Z-0781-2017)Nuvectra2016-12-17
Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500. For use recall (Z-1600-2016)Nuvectra2016-05-03

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Every clearance here is in the API, with alerts when new ones post.