It was reported that there was an issue with a vega knee components.It was reported that as a result of having the product implanted, the patient has experienced as vega knee loosing which results in a revision surgery.The primary surgery occurred on (b)(6) 2013 and revision surgery occurred on (b)(6) 2019.All available information has been provided at this time, if additional information becomes available the complaint will be updated accordingly.The adverse event / malfunction is filed under reference (b)(4).Involved components: nx029z (as vega ps femoral comp.Cemented f4n r), nx042 (patella 3-pegs p2), nx051z (as vega ps tibial plateau cemented t1), nx112(vega ps gliding surface t1/1+ 14mm), nn260p (plug f/tibial plateau).Associated medwatches: 2916714-2020-00453, 2916714-2020-00454, 2916714-2020-00455 , 2916714-2020-00456.
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