The patient was reportedly implanted with a biodesign or surgisis anterior pelvic floor graft, a biodesign or surgisis posterior pelvic floor graft, and a dima remeex system on (b)(6) 2011, at the (b)(6) by dr.(b)(6).The patient and her attorney have alleged that as a result of these products being implanted in the patient, the patient has experienced pain and injury.The following information was not provided by the complainant: specific information of the alleged injury.Specific information regarding whether intervention was performed.Specific information regarding why intervention was performed or what type/to what extent intervention was performed.Specific correlation between device performance and alleged injury.Current patient status.
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