The other 13 patient-specific events provided by this office are being reported separately.Since this event involved three medical devices, three manufacturer reports are being submitted.This report describes the second device.Manufacturer report numbers 3005174370-2015-00103 and 9611385-2015-00076, describe the first and third device, respectively.
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On (b)(6) 2015, a representative from the dental office provided patient-specific information; initially, this office indicated "a couple" of patients required root canal treatment.In total, the office has now provided information on 15 root canals involving 14 patients.This report details a (b)(6) male patient who received a crown made from 3m espe lava ultimate cad/cam restorative for cerec on tooth #31 on (b)(6) 2013.This crown was secured with 3m espe relyx ultimate adhesive resin cement and 3m espe scotchbond universal adhesive.On (b)(6) 2013, the crown debonded and was recemented.On (b)(6) 2014, the patient reported to the office that he was in pain and was referred for endodontic treatment.The endodontic procedure was performed on (b)(6) 2014; during the procedure, the crown debonded and was recemented.The patient's status is currently reported as fine.
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