WebThe Modular SMF and Modular REDAPT Hip System received fast-tracked approval through the FDA’s 510(k) process and were approved for sale in 2008 and 2012. Fast-tracked products are not typically ... WebAug 30, 2024 · The material properties of OXINIUM coupled with the design elements of LEGION™ Revision Knee System, LEGION HK Hinge Knee, OR3O™ Dual Mobility System and REDAPT™ Revision Hip System can bring...
REDAPT on Hip Replacement - Clinical Trials Registry - ICH GCP
WebSep 8, 2024 · The REDAPT Revision Hip System is distinctively designed to assist surgeons to tackle the challenges of revision hip arthroplasty: fixation in various bone types, … WebOct 2, 2015 · endoprosthesis, femoral osteotomy, or Girdlestone resection; fracture-dislocation of the hip; and correction of deformity. The REDAPT Porous Acetabular Shell is intended for single use only and is to be implanted without bone cement. The REDAPT Cemented Liner is intended for single use only and is to be implanted with bone cement. how they made the titanic movie
Short-term outcomes with the REDAPT monolithic, tapered
WebNov 17, 2016 · November 17, 2016. Smith & Nephew has recalled its Modular SMF and Modular Redapt hip implants due to an unprecedented complaint and adverse event trend with the modular necks used in the devices. Surgeons should monitor patients implanted with the Modular SMF and Modular Redapt hips for pain, swelling, limited mobility and … WebREDAPT Revision Acetabular System Developed for use where compromised bone makes total hip arthroplasty implant fixation and stability more difficult Brochure REDAPT Fully … WebSmith & Nephew Modular SMF and Modular Redapt Femoral System Recall UK-based Smith & Nephew launched its Modular SMF Hip System in 2008 and its Modular Redapt Femoral System in 2012. On November 15, 2016, the company recalled both hip implant systems because of large numbers of adverse events and complaints. metallica beer glass