It was reported that there was an issue with nk1003t - corehip std cementless 12/14 size 3.According to the complaint description, while placing the stem, a bone crack on the medial side of femur was observed.The stem was replaced with cemented non-aesculap stem.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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