It was reported via clinical evaluation report from a related research activity database (drra) that patients underwent an unknown procedure on unknown date and suture was used.The reported complication experienced by the following with corresponding intervention: 16,053 patients had bleeding peri-operative complication after the procedure with the use of the device and before the discharge of the index hospitalization.330 patients had wound disruption peri-operative complication after the procedure with the use of the device and before the discharge of the index hospitalization.1,255 patients had sepsis peri-operative complication after the procedure with the use of the device and before the discharge of the index hospitalization.432 patients had surgical site infection peri-operative complication after the procedure with the use of the device and before the discharge of the index hospitalization.No additional information was provided.
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