It was reported that there was an issue with as vega knee.It was reported that as a result of having the product implanted, the patient has experienced loosening which resulted in a revision surgery.The primary procedure occurred on (b)(6) 2013, and the revision was performed on (b)(6)2019.All available information has been provided at this time, if additional information becomes available the complaint will be updated accordingly.Involved components: as vega system ps, as patella p2, as vega ps tibial plateau cemented, as vega ps gliding surface t1/t1 + 12mm, as vega peek plug t1 - t5.The adverse event / malfunction is filed under reference (b)(4).Associated medwatches: 2916714-2020-00435, 2916714-2020-00436, 2916714-2020-00437, 2916714-2020-00438.
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