To date, the device has not been returned.If the product is returned for evaluation, any further information derived from the evaluation will be submitted in a supplemental 3500a form.Mwr (b)(4) submitted for adverse event which occurred on (b)(6) 2016.Mwr (b)(4) submitted for adverse event which occurred on (b)(6) 2017.
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It was reported by an attorney that the patient underwent hernia repair surgery on (b)(6) 2015 and mesh was implanted.It was reported that the patient underwent removal surgery and hernia repair surgery on (b)(6) 2016 and mesh was implanted.It was reported that the patient underwent laparoscopy with drainage of abscess on (b)(6) 2017.It was reported that the patient experienced severe pain, dense adhesions, nausea, diarrhea, chills, inflammation, drainage, abscess, loss of appetite and weight loss.Other procedure is captured under separate file.No additional information was provided.
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