Since this event involved four medical devices, four manufacturer reports are being submitted.This report describes the third device.Manufacturer report numbers 3005174370-2015-00126, 9611385-2015-00107, and 9611385-2015-00109 describe the first, second, and fourth device, respectively.
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On (b)(6) 2015, a dental assistant reported one patient who required a tooth extraction.The patient had a restoration made from 3m espe lava ultimate cad/cam restorative for cerec which was secured with 3m espe relyx ultimate adhesive resin cement, relyx univcem 2 cement and scotchbond universal adhesive.On (b)(6) 2015, it was reported that the doctor was not 100% sure that the extraction was due to the crown because there were other factors involved.
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