It was reported that there was an issue with as vega knee.As a result of having the product implanted the patient has experienced knee pain, swelling, difficulty walking, and loosening and instability of the implant.The primary surgery occurred on (b)(6) 2012 and the revision surgery occurred on (b)(6) 2016.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 xc (b)(4).Associated medwatches: 2916714-2020-00406, 2916714-2020-00407, 2916714-2020-00409, 2916714-2020-00410.Involved components: nx011z (ps femur cemented f5n lt) nn260p (peek plug f/ tibia) nx053z (ps tibia cemented t2) nx044 (universal patella p4) nx120 (ps pe insert t2/t2+, 10mm) the cement used is unidentified.
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