Bryan cervical disc
WebApr 23, 2015 · Heller, J G Sasso, R C Papadopoulos, S M , et al. Comparison of Bryan cervical disc arthroplasty with anterior cervical decompression and fusion: clinical and radiographic results of a randomized, controlled, clinical trial Spine (Phila Pa 1976) 2009 34 2 … WebThe Bryan Cervical Disc System (Medtronic), approved by the FDA in 2012, consists of two titanium alloy shells with a polyurethane nucleus . A polyurethane sheath surrounds the nucleus for an enclosed articulating environment. Sterile saline is injected into the sheath as a lubricant. Unique ...
Bryan cervical disc
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WebSep 15, 2011 · In vitro biomechanical comparison of cervical disc arthroplasty, ventral slot procedure, ... Lin CY, Kang H, Rouleau JP, et al. Stress analysis of the interface between cervical vertebrae and end plates and the Bryan, Prestige LP, and ProDisc-C cervical disc prostheses: an in vivo image-based finite element study. Spine (Phila Pa 1976) ... WebMay 25, 2007 · The Bryan Cervical Disc is designed to alleviate pain and preserve motion and flexibility while replacing a diseased disc that is removed from a patient’s cervical spine. Traditionally, the most ...
WebIntroduction. Anterior cervical discectomy and fusion (ACDF) is used to treat cervical degenerative disc disease and has proved clinically efficacious. 1,2 Yet an alternative to … WebJan 27, 2016 · Bryan Cervical Disc Prosthesis made by Medtronic Sofamor Danek (Memphis, Tennessee) consists of a nucleus made of polyurethane between two titanium alloy endplates in a clamshell configuration. The two bearing surfaces in the arthroplasty at the interfaces between the nucleus and the endplates are contained by a polyurethane …
WebAbstract. Preserving the function of cervical disc prostheses, even over the short term, is a matter of concern among surgeons. Our case series highlights our results and protocol for increasing the probability of continued device function. Twenty-five consecutive patients with a mean (+/-SEM) age of 44.3+/-8.3 years underwent 29 cervical total ... WebIntroduction. Anterior cervical discectomy and fusion (ACDF) is used to treat cervical degenerative disc disease and has proved clinically efficacious. 1,2 Yet an alternative to fusion is Bryan cervical disc arthroplasty (BCDA), which preserves motion of the cervical disc and decreases the incidence of surgical and adjacent segment degeneration (SASD).
WebThe FDA's approval of the Bryan Cervical Disc was based upon the results of a clinical trial (non-inferiority) involving 463 patients at 30 clinical sites comparing the Bryan device to ACDF. Patients with intractable radiculopathy and/or myelopathy resulting in impaired function with at least one clinical neurological sign associated with the ...
WebBackground: The CTDR is a technique that treats cervical disc degenerative disease. Initial shorter-term studies showed good clinical and radiological results. Purpose: To assess … simply forms brooklyn nyWebJul 6, 2024 · A sterile orthopaedic surgical instrument designed to cut and resurface with precision, the opposing endplates of adjacent cervical vertebrae, for the acceptance of … simply formulary 2022WebJul 10, 2024 · In 2009, the Bryan Cervical Disc was approved by the FDA for treatment using an anterior approach of single-level cervical degenerative disc disease defined as … rays tent city nunawadingWebBryan cervical disc system (Medtronic Sofamor Danek, Memphis, TN, USA). Patients and methods Patient population We performed 46 arthroplasties using the Bryan disc from 2003 to 2005. The study ... rays tent city geelongWebNov 2, 2016 · The Bryan disc is a metal-on-plastic design (titanium and polyurethane). The PRESTIGE® Cervical Disc is a metal-on-metal design (stainless steel) that has undergone a long history of evolution ... simply formationWebThe BRYAN Cervical Disc is made of two metal (titanium) shells and a mobile inner polyurethane (plastic) core. It is designed to provide motion by allowing movement between the two metal components and the plastic … simply formsWebthe cervical level to be treated, and necessitating surgery as demonstrated using computed tomography, myelography and computed tomography, and/or magnetic resonance imaging results. Patients receiving the Bryan® Cervical Disc should have failed at least six weeks of nonoperative treatment before implantation. rays tents