It was reported that there was an issue with nk1044t - corehip var cementless 12/14 size 4.According to the complaint description, while placing the stem, a bone fracture was observed.Wiring was fixed and the surgery was successfully completed.The surgeon had not recognized the osteotomy line and coating line.According to manufacturer's reporting evaluation in accordance with 21 cfr part 803, section 803.3, this event is considered reportable for the following reason - adverse event (not later than 30 days).The assessment for the reportability of this adverse event was based on the patient harm, additional medical intervention.Additional information was not provided nor available.The adverse event is filed under aesculap ag reference no.(b)(4).
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