Stryker LFIT Femoral Heads | 合法醫療器材資訊網
TheLFIT("LowFrictionIonTreatment")V40FemoralHeadiscompatiblewithmanydifferentmodelsofcommerciallyavailableStrykerfemoralstemsincludingthe ...
Another Defective Hip Recall from StrykerAnother recall[1] announcement was made by Stryker Orthopaedics[2] in August of 2016 regarding the companys line of LFIT V40 femoral heads manufactured before 2011. On August 29, 2016, Stryker sent an "Urgent Medical Device Recall Notification" letter[3] to surgeons. The letter explained Stryker had received higher than normal problems involving taper lock failure with the recalled femoral heads. The taper lock is the part of the hip device that connects the femoral head to the femoral neck during total hip replacement procedures. The LFIT ("Low Friction Ion Treatment") V40 Femoral Head is compatible with many different models of commercially available Stryker femoral stems including the Accolade TMZF[4] and Secur-Fit Max[5]. The estimated number of Stryker LFIT...
LFIT Anatomic CoCr V40 femoral heads | 合法醫療器材資訊網
MDL 2768 | 合法醫療器材資訊網
Stryker Adds LFIT V40 Hip Replacement Parts to Safety Alert | 合法醫療器材資訊網
Stryker LFIT CoCr V40 Femoral Heads | 合法醫療器材資訊網
Stryker LFIT Femoral Heads | 合法醫療器材資訊網
Stryker LFIT V40 Femoral Head Artificial Hip Recall ... | 合法醫療器材資訊網
Stryker LFIT V40 Femoral Head Lawsuit | 合法醫療器材資訊網
Stryker LFIT V40 Femoral Head Recall & Lawsuits | 合法醫療器材資訊網
Stryker LFIT V40 Femoral Head Recall 2016 | 合法醫療器材資訊網
Stryker® Orthopedics LFIT™ CoCr V40™ Femoral Head ... | 合法醫療器材資訊網
【“史賽克”股骨頭】許可證字號:衛部醫器輸字第029701號
器材品名:“史賽克”股骨頭許可證字號:衛部醫器輸字第029701號註銷狀態:註銷日期:註銷理由:有效日期:2022/04/26發證日期:2017/...
【“好美得卡 奧斯得寧”人工股骨頭】許可證字號:衛署醫器輸字第019147號
器材品名:“好美得卡奧斯得寧”人工股骨頭許可證字號:衛署醫器輸字第019147號註銷狀態:註銷日期:註銷理由:有效日期:2023/08/01...