Sentence examples for femoral device from inspiring English sources

The femoral device used was a CMK in 14 hips, and a PHS 6 in 13 hips.

We evaluated the safety and efficacy after hemostasis with our locally designed Assiut femoral compression device (AFCD) versus manual compression after diagnostic coronary angiography at Assiut University Hospitals.

This study was performed to evaluate the safety and efficacy of a locally designed assiut femoral compression device (AFCD) versus manual compression (MC).

This study was performed to evaluate the feasibility and safety of early sheath removal after percutaneous coronary intervention (PCI) using a locally designed Assiut Femoral Compression Device (AFCD2) vs. manual compression (MC).

Further studies are needed to verify whether the femoral closure device will have an impact on femoral artery positive remodelling.

Previous studies may have measured the metal interference screw position or the femoral aiming device position, which, however, need not correlate with the actual tunnel or graft position (Klos et al. 2000).

Despite the inclusion of longer lesion lengths that are at a higher risk of treatment failure, the 2.4% target lesion revascularization rate is the lowest reported for a superficial femoral artery device trial at 12 months.

Some femoral sizing devices allow rotational adjustment before sizing (rotation-modified sizing devices), while others do not (rotation-unmodified sizing devices).

Several femoral fixation devices are available for hamstring tendon autograft in anterior cruciate ligament (ACL) reconstruction, but the best technique is debatable.

Nine different femoral fixation devices were tested and classified according to their fixation mechanism: compression (Bioscrew and RCI screw); expansion (Rigidfix); cortical suspension (Ligament Anchor, EndoButton-CL, and Swing Bridge); cancellous suspension (Linx-HT); and cortical-cancellous suspension (Transfix and Bio-Transfix).

Since we did not have baseline ultrasound of bilateral femoral arteries before device deployment, we cannot ascertain whether the discrepancy is due to nature difference or device-related injury and positive remodelling.