Mobi c - Sep 27, 2019 · Mobi-C group composed of 15 subjects, in which 6 were male and 9 were female. There were no statistical differences in demographics and baseline characteristics of subjects between the M6-C and Mobi-C groups, including age, gender, BMI, smoking history, the type of surgery, ROM and FSU height ( Table 7 ).

 
Product Usage: The device is intended as a cervical intervertebral disc replacement at one or two contiguous levels from C3 to C7 designed to maintain/restore segmental motion and disc height. MOBI-C distraction pins are inserted into the vertebral body below and above the disc that is to have the disc replacement.. Projectidproviderinterface

The Mobi-C Two-Level Study 5-Year Results This is a prospective, randomized, FDA supervised IDE study which is designed for a 7-year follow-up. At the 2-year and 5-year marks, Mobi-C demonstrated fewer subsequent surgeries, lower rates of adverse events, lower rates of adjacent level degeneration, and higher NDI (neck disability index) success ...May 1, 2018 · Mobi-C discs from 16 patients and M6-C discs from 56 patients, both MoP implants, were compared in terms of the range of motion by Pham et al. [20]. A range of motion of 14.2 °± 5.1 °for Mobi-C ... Mobi-C – How it Works. Mobi-C contains patented mobile bearing technology that allows the polyethylene core to slide and rotate inside the disc for self-adjustment to the cervical spine movements. This means that Mobi-C can react to the normal motion in the cervical spine.Product Usage: The device is intended as a cervical intervertebral disc replacement at one or two contiguous levels from C3 to C7 designed to maintain/restore segmental motion and disc height. MOBI-C distraction pins are inserted into the vertebral body below and above the disc that is to have the disc replacement.Jul 31, 2020 · The replacement Mobi-C device has not failed to date, unlike the first Mobi-C device, which failed 1 week postoperatively in this same patient. This result likely rules out patient factors as the underlying cause of failure and may speak to the increased need to have a very precise surgical technique to prevent anterior slippage of the endplate ... Nov 15, 2021 · The Mobi-C device was thought by the plaintiff to be flawed since it differed from the device that the Food and Drug Administration had approved, which affect the “safety and efficacy of the ... Mobi-C is the first cervical disc FDA approved for both one and two-level indications, and is used to help minimize pain and symptoms associated with bulging or diseased cervical discs. During an artificial disc replacement, the diseased disc will be replaced with the Mobi-C prosthetic disc to restore disc height and the distance between two ...About Mobi-C. What is the Mobi-C Cervical Disc? How does Mobi-C Compare to Fusion? Who Should Receive a Mobi-C? Complications & Precautions; What are the 10 year clinical results? Insurance Coverage; Real Experiences; Am I a Candidate? Surgeon Locator; Contact; I am a Surgeon. Clinical Results; Surgeon Testimonials; Press Kit; Insurance ...• A single Mobi-C prosthesis costs £1,750 (excluding VAT). Two Mobi-C devices are needed for 2-level cervical disc replacement. • A US cost-effectiveness analysis found that the average cost per patient in the 5 years after surgery was $23,459 (about £16,515) for Mobi-C, and $21,772 (about £16,031) for ACDF. Apr 13, 2020 · Zimmer Biomet Spine has announced that over 150,000 Mobi-C Cervical Discs have been implanted worldwide. The implant, a cobalt chromium alloy and polyethylene mobile-bearing prosthesis, was first implanted in France in 2004 and was approved for sale in the U.S. by the FDA in 2013. Noting the bulwark of data on the device, James Cloar, President ... The Mobi-C has three parts: two metal plates and a medical grade polyethylene insert in the middle. The top plate rotates over the domed insert. The insert slides across the bottom plate, left-to-right and front-to-back up to 1mm in any direction. The insert also twists over the bottom plate. The two tabs on the bottom plate provide a safety ... Aug 28, 2020 · The objective is to report a case of an early dislocation of Mobi-C prosthesis used for the replacement of C4–C5 disc. A 57-year-old man who was operated 17 years before for C6–C7 fusion complained of cervicalgia associated with bilateral but predominantly right-sided brachialgia. Magnetic resonance imaging demonstrated central and ... Mobi-C implant surgery is a safe alternative to ACDF surgery in cervical disc degeneration. Cite this article: Bone Joint J 2016;98-B:829-3. Effectiveness and safety of Mobi-C for treatment of single-level cervical disc spondylosis: a randomised control trial with a minimum of five years of follow-upThe Mobi-C cervical disc is one of the most widely used cervical discs in the world. Mobi-C contains patented Mobile Core Technology™ that allows the polyeth...The objective is to report a case of an early dislocation of Mobi-C prosthesis used for the replacement of C4–C5 disc. A 57-year-old man who was operated 17 years before for C6–C7 fusion complained of cervicalgia associated with bilateral but predominantly right-sided brachialgia. Magnetic resonance imaging demonstrated central and ...May 01, 2019. SAN DIEGO — Improvements were sustained at 10 years for patients treated with the Mobi-C cervical disc in the trial that led to its approval by the US Food and Drug Administration ...The Mobi-C device was thought by the plaintiff to be flawed since it differed from the device that the Food and Drug Administration had approved, which affect the “safety and efficacy of the ...The following conclusions can be drawn from the present study review: 1) one-level Mobi-C CDA is non-inferior, but not superior, to one-level ACDF for patients with cervical DDD; 2) the Mobi-C CDA procedure is associated with high rates of HO; and 3) two-level Mobi-C CDA may be superior to two-level ACDF, but substantial evidence is lacking ...Zip. Institution. Map. Details. Email These Surgeons to Me. Zimmer Biomet is pleased to provide the Surgeon Locator to allow you to find surgeons who have been trained on Mobi-C. This locator may not be a complete list of trained surgeons in your area, and Zimmer Biomet does not make any recommendation or referral regarding the proper facility ... Apr 28, 2016 · Mobi-C® Cervical Disc is the first and only neck surgery prosthesis approved for reconstruction of the disc(s) from C3-C7 following discectomy at one or two ... Had Mobi-C disc put in at C5-C6, however 1st surgery failed to remove bone spur sticking into my spinal cord. 2nd surgery took care of it. Recommend using Yelp or other online reviews of doctors ...Mobi-C is a cobalt chromium alloy and polyethylene mobile-bearing prosthesis that is inserted in a single step, without requiring bone chiseling or other vertebral anchorage such as screws or keels.Mobi-C Cervical Disc is an artificial disc that can replace a worn or degenerative disc. This surgery helps provide both lateral and vertical range of motion along with maintaining neck rotation. This differs from spinal fusion surgery when two of the vertebrae are fused together with hardware, which constricts the neck’s range of motion. Mobi-C provides bone sparing fixation without chisel cuts into the small vertebral bodies of the cervical spine, making it safe for implantation at two levels. About Mobi-C Disc Replacement Mobi-C Disc Replacement is performed under general anesthesia, usually as an outpatient procedure. Mobi-C is non-inferior to ACDF at one level and superior at two levels2 Mobi-C had lower rates of adjacent segment degeneration at 84 months Mobi-C had fewer subsequent surgeries at 84 months One-level deterioration of adjacent segments at 84 months compared to baseline: • 43.8% for Mobi-C compared to 63.0% for ACDF at the inferior level.The Mobi-C ® Cervical Disc Prosthesis is indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following discectomy at one level or two contiguous levels for intractable radiculopathy (arm pain and/or a neurological deficit) with or without neck pain, or myelopathy due to abnormality localized to the level of the disc space and at least one of the following ...Aug 7, 2013 · Figure 2. Degrees of Freedom of the Mobi-C® The inferior endplate includes two lateral stops that control and limit the translation and rotation of the mobile insert. The lateral stops also prevent the potential for migration of the mobile insert. Mobi-C® is designed to control the amount of translation by the mobile insert in the X Only 1 study analyzed outcomes of 1-level versus 2-level Mobi-C CDA, and only 1 study analyzed 2-level Mobi-C CDA versus 2-level ACDF. In comparison with other cervical disc prostheses, the Mobi-C prosthesis is associated with higher rates of heterotopic ossification (HO). Studies with conflicts of interest reported lower rates of HO.Only 1 study analyzed outcomes of 1-level versus 2-level Mobi-C CDA, and only 1 study analyzed 2-level Mobi-C CDA versus 2-level ACDF. In comparison with other cervical disc prostheses, the Mobi-C prosthesis is associated with higher rates of heterotopic ossification (HO). Studies with conflicts of interest reported lower rates of HO.Mobi-C® Cervical Disc. The upper and lower bone-facing endplates of the Mobi-C® Cervical Disc are made of a cobalt chromium molybdenum alloy. The endplates are coated with a fine layer of titanium and hydroxyapatite to promote integration with bone. Jul 31, 2020 · Here, the authors present a series of 4 patients initially treated with Mobi-C artificial disc implants who developed postoperative neck pain. Dynamic imaging revealed segmental kyphosis at the level of the implant. All implants were locked in the flexion position, and all patients required reoperation. This is the first reported case series of ... The average return to work time was 20.9 days shorter for Mobi-C compared to ACDF. The patients in this study will continue to be followed for 7 years after surgery. The clinical benefit beyond five years has not been measured. To find a trained Mobi-C surgeon, please visit the surgeon locator. Potential adverse effects from surgery with the Mobi-CThe Mobi-C differs from some other contemporary disc designs in that it has a mobile polyethylene insert that is sandwiched between superior and inferior cobalt chromium endplates. While some studies claim the Mobi-C to have restored normal cervical spinal biomechanics, others have noted high levels of migration.1. "Looks like the Mobi-C failed, replace it with a ProDisc or try a fusion without a plate at one level. Unclear of which approach would be best", recommended me to a specialist in ADR more verse in this case. (Orthopedic Spine surgeon from TN) 2. Surgeon that was referred to me by the above. "Mobi-C failed, causing instability and hypermobility.Two-level CDA with the Mobi-C® device demonstrated equivalent, and in certain aspects, favorable outcomes compared to ACDF for treatment of symptomatic cervical 2-level degenerative disc disease (DDD) indicating a satisfactory safety and efficacy profile.Apr 28, 2016 · Mobi-C® Cervical Disc is the first and only neck surgery prosthesis approved for reconstruction of the disc(s) from C3-C7 following discectomy at one or two ... Mobi-C is a cobalt chromium alloy and polyethylene mobile-bearing prosthesis that is inserted in a single step, without requiring bone chiseling or other vertebral anchorage such as screws or keels.The Mobi-C device was thought by the plaintiff to be flawed since it differed from the device that the Food and Drug Administration had approved, which affect the “safety and efficacy of the ...Apr 13, 2020 · Zimmer Biomet Spine has announced that over 150,000 Mobi-C Cervical Discs have been implanted worldwide. The implant, a cobalt chromium alloy and polyethylene mobile-bearing prosthesis, was first implanted in France in 2004 and was approved for sale in the U.S. by the FDA in 2013. Noting the bulwark of data on the device, James Cloar, President ... Mobi-C Had Lower Rates of Adjacent Segment Degeneration at 84 Months Mobi-C Had Fewer Subsequent Surgeries at 84 Months The ONE-LEVEL deterioration of adjacent segments at 84 months compared to baseline was: • 43.8% for Mobi-C compared to 63.0% for ACDF at the inferior level. • 40.4% for Mobi-C compared to 65.1% for ACDF Nov 28, 2017 · One limitation of this study was the specific inclusion and exclusion criteria for entry into the study. At the time of conception, the intention of the Mobi-C study was to enroll patients without significant conditions that could confound the outcome of an artificial disc. Page 1 of 7 Last Updated 01-DECEMBER-2022 . Zimmer Biomet Patent Marking . This information is provided as notice of patented articles pursuant to 35 U.S.C. § 287(a).Apr 3, 2023 · Mobi-C is a cobalt chromium alloy and polyethylene mobile-bearing prosthesis that is inserted in a single step, without requiring bone chiseling or other vertebral anchorage such as screws or keels. The Mobi-C ® Cervical Disc Prosthesis is indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following discectomy at one level or two contiguous levels for intractable radiculopathy (arm pain and/or a neurological deficit) with or without neck pain, or myelopathy due to abnormality localized to the level of the disc space and at least one of the following ... The Mobi-C cervical artificial disc (LDR Medical; Troyes, France) is a semiconstrained, mobile bearing, bone-sparing TDR consisting of 2 cobalt–chromium–molybdenum alloy endplates and an ultra-high-molecular-weight polyethylene mobile insert facilitating 5 independent degrees of freedom.Mobi-C provides bone sparing fixation without chisel cuts into the small vertebral bodies of the cervical spine, making it safe for implantation at two levels. About Mobi-C Disc Replacement Mobi-C Disc Replacement is performed under general anesthesia, usually as an outpatient procedure. LDR Spine –Mobi-C® P110009 Page 3 of 82 The Mobi-C® endplates are available in seven footprint sizes to address individual patient anatomy and maximize endplate coverage. These sizes are illustrated in the table below. Table 1. Mobi-C® Device Configurations Depth x Width (mm) Inferior/Superior Plate & Mobile Insert Sizes Combinations ... The average return to work time was 20.9 days shorter for Mobi-C compared to ACDF. The patients in this study will continue to be followed for 7 years after surgery. The clinical benefit beyond five years has not been measured. To find a trained Mobi-C surgeon, please visit the surgeon locator. Potential adverse effects from surgery with the Mobi-CCervical disc replacement surgery is designed to replace a damaged spinal disc in the neck with an artificial disc implant. Damaged cervical discs are most likely to occur at the C4-C5, C5-C6, or C6-C7 levels.Objective: Mobi-C cervical disc arthroplasty (MCDA) is an alternative to anterior cervical discectomy and fusion (ACDF). This study evaluated the effectiveness and safety of MCDA and ACDF for symptomatic cervical degenerative disc disease. What is Mobi-C. Mobi-C is the first cervical disc in the U.S. approved to treat more than one level of the cervical spine. It received FDA approval for one and two-level indications in August 2013. Mobi-C demonstrated statistical superiority compared to cervical spine fusion in overall study success when used in two-level patients at 5 years.Mobi-C discs from 16 patients and M6-C discs from 56 patients, both MoP implants, were compared in terms of the range of motion by Pham et al. [20]. A range of motion of 14.2 °± 5.1 °for Mobi-C ...The Mobi-C cervical artificial disc (LDR Medical; Troyes, France) is a semiconstrained, mobile bearing, bone-sparing TDR consisting of 2 cobalt–chromium–molybdenum alloy endplates and an ultra-high-molecular-weight polyethylene mobile insert facilitating 5 independent degrees of freedom.However, Mobi-C disc replacement is very different in a number of ways. The purpose of the replacement surgery is obviously to replace the damaged disc and help with neck pain, arm pain, and arm tingling, for instance. However, the device is designed to promote neck movement (including turning left-to-ride, bending side-to-side, and bending ... In 2015, FDA approved an update to the Mobi-C labeling to include five year clinical results. Of note, Mobi-C demonstrated superiority at all time points to five years on overall trial success as compared to two-level ACDF. The Mobi-C consists of two cobalt chromium (CoCr) endplates that are plasma sprayed with titanium Mobi-C is the first cervical disc FDA approved for both one and two-level indications, and is used to help minimize pain and symptoms associated with bulging or diseased cervical discs. During an artificial disc replacement, the diseased disc will be replaced with the Mobi-C prosthetic disc to restore disc height and the distance between two ... Mobi-C provides bone sparing fixation without chisel cuts into the small vertebral bodies of the cervical spine, making it safe for implantation at two levels. About Mobi-C Disc Replacement Mobi-C Disc Replacement is performed under general anesthesia, usually as an outpatient procedure.Page 1 of 7 Last Updated 01-DECEMBER-2022 . Zimmer Biomet Patent Marking . This information is provided as notice of patented articles pursuant to 35 U.S.C. § 287(a).Mobi-C implant surgery is a safe alternative to ACDF surgery in cervical disc degeneration. Cite this article: Bone Joint J 2016;98-B:829-3. Effectiveness and safety of Mobi-C for treatment of single-level cervical disc spondylosis: a randomised control trial with a minimum of five years of follow-upThe Mobi-C Cervical Disc has been designed for cervical disc replacement to restore segmental motion and disc height. The components of Mobi-C include superior and inferior cobalt chromium molybdenum alloy endplates coated with plasma sprayed titanium and hydroxyapatite coating, and a polyethylene mobile bearing insert.Return to Mobi-C Homepage If unsure about the answers to these questions, please consult with your doctor about your condition. This is for educational purposes only and is not meant to replace a conversation with and examination by a qualified physician.Zip. Institution. Map. Details. Email These Surgeons to Me. Zimmer Biomet is pleased to provide the Surgeon Locator to allow you to find surgeons who have been trained on Mobi-C. This locator may not be a complete list of trained surgeons in your area, and Zimmer Biomet does not make any recommendation or referral regarding the proper facility ...The Mobi-C Cervical Disc is implanted using an anterior approach. Patients should have failed at least 6 weeks of conservative treatment or demonstrated progressive signs or symptoms despite nonoperative treatment prior to implantation of the Mobi-C Cervical Disc. Physician CPT® Code CPT Description Insertion 22856The Mobi-C is composed of three parts—two metal plates that sandwich a plastic insert. While other artificial discs require neurosurgeons to chisel bone and drill screws to hold the device in place, the Mobi-C has teeth on the top and bottom to secure the plates to the vertebrae on either side.Mobi-C implant surgery is a safe alternative to ACDF surgery in cervical disc degeneration. Cite this article: Bone Joint J 2016;98-B:829-3. Effectiveness and safety of Mobi-C for treatment of single-level cervical disc spondylosis: a randomised control trial with a minimum of five years of follow-up Mobi-C Cervical Disc Mobi-C is the first cervical disc prosthesis approved by the FDA for reconstruction of a cervical disc at both one and two levels (C3-C7). Mobi-C is a cobalt chromium alloy and polyethylene mobile-bearing prosthesis that is inserted in a single step, without requiring bone chiseling to accommodate vertebral anchorage such as screws or keels.MOBI-C® prosthesis is a device for cervical intervertebral disc replacement (C3/C4, C4/C5, C5/C6, C6/C7) in order to restore segmental motion and disc height. Before any surgical procedure, read carefully the instructions and the surgical technique. Open the catalog to page 1. SURGICAL TECHNIQUE Pre-operative considerations Implant height ... The Mobi-C Cervical Disc. ZimVie Inc. has marked a major milestone with its Mobi-C Cervical Disc, announcing that more than 200,000 discs have been implanted worldwide. The total includes patients treated in more than 25 countries since the first surgery in France 19 years ago. In 2013, Mobi-C became the first cervical disc to win approval from ...The Mobi-C device was thought by the plaintiff to be flawed since it differed from the device that the Food and Drug Administration had approved, which affect the “safety and efficacy of the ...Objective: Mobi-C cervical disc arthroplasty (MCDA) is an alternative to anterior cervical discectomy and fusion (ACDF). This study evaluated the effectiveness and safety of MCDA and ACDF for symptomatic cervical degenerative disc disease.The Mobi-C has three parts: two metal plates and a medical grade polyethylene insert in the middle. The top plate rotates over the domed insert. The insert slides across the bottom plate, left-to-right and front-to-back up to 1mm in any direction. The insert also twists over the bottom plate. The two tabs on the bottom plate provide a safety ... 1. "Looks like the Mobi-C failed, replace it with a ProDisc or try a fusion without a plate at one level. Unclear of which approach would be best", recommended me to a specialist in ADR more verse in this case. (Orthopedic Spine surgeon from TN) 2. Surgeon that was referred to me by the above. "Mobi-C failed, causing instability and hypermobility.May 01, 2019. SAN DIEGO — Improvements were sustained at 10 years for patients treated with the Mobi-C cervical disc in the trial that led to its approval by the US Food and Drug Administration ...The Mobi-C Cervical Disc is implanted using an anterior approach. Patients should have failed at least 6 weeks of conservative treatment or demonstrated progressive signs or symptoms despite nonoperative treatment prior to implantation of the Mobi-C Cervical Disc. Physician CPT® Code CPT Description Insertion 22856The average return to work time was 20.9 days shorter for Mobi-C compared to ACDF. The patients in this study will continue to be followed for 7 years after surgery. The clinical benefit beyond five years has not been measured. To find a trained Mobi-C surgeon, please visit the surgeon locator. Potential adverse effects from surgery with the Mobi-CObjective: Mobi-C cervical disc arthroplasty (MCDA) is an alternative to anterior cervical discectomy and fusion (ACDF). This study evaluated the effectiveness and safety of MCDA and ACDF for symptomatic cervical degenerative disc disease.The average return to work time was 20.9 days shorter for Mobi-C compared to ACDF. The patients in this study will continue to be followed for 7 years after surgery. The clinical benefit beyond five years has not been measured. To find a trained Mobi-C surgeon, please visit the surgeon locator. Potential adverse effects from surgery with the Mobi-CMobi-C is the only device to have FDA approval for treatment of two-level cervical disc disease. The data from these trials demonstrated that Mobi-C results in clinically superior outcomes as compared to ACDF for treatment of two-level cervical disc disease. Mobi-C FDA Pivotal Clinical Trials and Post-Approval Study (Mobi-C vs. ACDF)The primary objective of this study was to rigorously compare the Mobi-C cervical artificial disc to ACDF for treatment of cervical DDD at 2 contiguous levels of the cervical spine. Methods: This study was a prospective, randomized, US FDA investigational device exemption pivotal trial of the Mobi-C cervical artificial disc conducted at 24 ... 詳細. 移動式インサートの可動性を制御することは、Mobi-C® ディスクプロテーゼの基礎です。. この第 2 世代の人工椎間板は、脊髄関節形成術を専門とする外科医のチームによって設計されました。. Mobi-Cはユニークで信頼性が高く、特許取得済みの移植 ...Apr 13, 2020 · Zimmer Biomet Spine has announced that over 150,000 Mobi-C Cervical Discs have been implanted worldwide. The implant, a cobalt chromium alloy and polyethylene mobile-bearing prosthesis, was first implanted in France in 2004 and was approved for sale in the U.S. by the FDA in 2013. Noting the bulwark of data on the device, James Cloar, President ... What is Mobi-C. Mobi-C is the first cervical disc in the U.S. approved to treat more than one level of the cervical spine. It received FDA approval for one and two-level indications in August 2013. Mobi-C demonstrated statistical superiority compared to cervical spine fusion in overall study success when used in two-level patients at 5 years.

Seven patients (3%) treated with Mobi-C and twelve patients (11%) treated with ACDF, had surgery at an adjacent level within 5 years after surgery. No mechanical failures of the Mobi-C device were observed in any study patients. A comprehensive list of risks is provided in the package insert for the device, which your doctor has received.. 20191205_sentiment_veroffentlichung_in_liquidation.pdf

mobi c

In 2015, FDA approved an update to the Mobi-C labeling to include five year clinical results. Of note, Mobi-C demonstrated superiority at all time points to five years on overall trial success as compared to two-level ACDF. The Mobi-C consists of two cobalt chromium (CoCr) endplates that are plasma sprayed with titanium Mobi-C provides bone sparing fixation without chisel cuts into the small vertebral bodies of the cervical spine, making it safe for implantation at two levels. About Mobi-C Disc Replacement Mobi-C Disc Replacement is performed under general anesthesia, usually as an outpatient procedure. Sep 7, 2022 · 1. "Looks like the Mobi-C failed, replace it with a ProDisc or try a fusion without a plate at one level. Unclear of which approach would be best", recommended me to a specialist in ADR more verse in this case. (Orthopedic Spine surgeon from TN) 2. Surgeon that was referred to me by the above. "Mobi-C failed, causing instability and hypermobility. The Mobi-C disc is one of the most common options for replacement cervical discs around the world. The medical device was first used in 2004 and has continued to be used successfully in patients with cervical disc issues (that is, disc issues in the neck). Without a doubt, many people who have undergone a Mobi-C disc procedure have had ...About Mobi-C. What is the Mobi-C Cervical Disc? How does Mobi-C Compare to Fusion? Who Should Receive a Mobi-C? Complications & Precautions; What are the 10 year clinical results? Insurance Coverage; Real Experiences; Am I a Candidate? Surgeon Locator; Contact; I am a Surgeon. Clinical Results; Surgeon Testimonials; Press Kit; Insurance ...Results: There was no statistical significance in the difference of overall flexion range between M6-C and Mobi-C prostheses. However, overall range of extension of Mobi-C was greater compared to M6-C (P = 0.028). At C 5-6, the range of flexion for both implants were similar but lesser compared to asymptomatic patients (P < 0.001). Range of ... Mar 28, 2018 · Mobi-C Cervical Disc Mobi-C is the first cervical disc prosthesis approved by the FDA for reconstruction of a cervical disc at both one and two levels (C3-C7). Mobi-C is a cobalt chromium alloy and polyethylene mobile-bearing prosthesis that is inserted in a single step, without requiring bone chiseling to accommodate vertebral anchorage such as screws or keels. In a surgery with the Mobi-C Cervical Disc, the unhealthy disc is removed, but instead of a bone spacer or plastic implant along with a plate and screws, a Mobi-C is implanted into the disc space. Where a fusion procedure is intended to eliminate motion at the surgery levels, the goal of a surgery with Mobi-C is to allow motion at those levels. Glossary annulus fibrosus - The outer protective ring of a spinal disc, which covers the soft center (nucleus pulposus).Made from strong rings of fibers. ACDF - Anterior cervical discectomy and fusion (ACDF) is aIn a surgery with the Mobi-C Cervical Disc, the unhealthy disc is removed, but instead of a bone spacer or plastic implant along with a plate and screws, a Mobi-C is implanted into the disc space. Where a fusion procedure is intended to eliminate motion at the surgery levels, the goal of a surgery with Mobi-C is to allow motion at those levels.The Mobi-C Cervical Disc is now available to more than 200 million insured patients with one-level disc disease and more than 150 million patients with two-level disc disease across more than 90 commercial insurance plans. That makes Mobi-C the most widely covered intervertebral disc for cervical disc replacement in the industry.Nov 28, 2017 · Ethical standards: The Mobi-C Clinical Trial (ClinicalTrials.gov registration number: NCT00389597) was conducted at 24 sites in the US and was approved by the Institutional Review Board, Research Ethics Committee, or local equivalent of each participating site. Level of evidence: 1. The average return to work time was 20.9 days shorter for Mobi-C compared to ACDF. The patients in this study will continue to be followed for 7 years after surgery. The clinical benefit beyond five years has not been measured. To find a trained Mobi-C surgeon, please visit the surgeon locator. Potential adverse effects from surgery with the Mobi-CIn 2015, FDA approved an update to the Mobi-C labeling to include five year clinical results. Of note, Mobi-C demonstrated superiority at all time points to five years on overall trial success as compared to two-level ACDF. The Mobi-C consists of two cobalt chromium (CoCr) endplates that are plasma sprayed with titanium.

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