WebNov 15, 2012 · "REDAPT changes these outcome expectations to include the type of functional standards typically associated with primary total hip replacements. And, it does … 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.

Smith & Nephew SMF Hip System and REDAPT Recall Lawyers

WebREDAPT Indications. Hip components are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or noninflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, … WebRedapt Modular Sleeved Revision Hip Stems and size 26/27 Modular Sleeves are substantially equivalent to the MDF Revision Hip Stems and modular sleeves cleared by premarket notification K(081124. Giving consideration to the device modifications described in the Device Description section, no changes have microsoft teams room update manually

REDAPT on Hip Replacement - Clinical Trials Registry - ICH GCP

WebREDAPT is a tapered, forged titanium stem with proprietary ROCKTITE distal flutes for improved diaphyseal fixation. REDAPT is available in two stem styles — Proximally Fluted … WebDec 1, 2016 · Fact Checked. UK-based medical device company Smith & Nephew announced a recall of its Modular SMF and Modular Redapt hip implants after it received reports of … WebModular SMF and Modular Redapt Femoral Hip Systems Smith & Nephew recalled the modular SMF and Redapt Femoral Hip Systems in 2016. They also recalled the corresponding hip stem components because the … microsoft teams room update process