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. The Mobi-C Cervical Disc is one of the most widely used cervical discs in the world. First implanted in France in November 2004, Mobi-C has now been implanted in more than 75,000 spinal levels in 25 countries. Mobi-C is intended for adult patients (skeletally mature) with arm pain and/or neurological symptoms (such as weakness or numbness) with ...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. Mobi C Artificial Disc New research studies by the North American Spine Society — the most respected international society of spine surgeons — have shown that when a person has a herniated disc in the neck, and traditional fusion surgery is performed, there is an increased incidence of herniation at an adjacent segment.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 ... 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 ...Restoring natural motion to the cervical spine. The controlled mobility of the patented mobile core is the foundation of Mobi-C. With vertebrae and neck muscle movement, the Mobi-C implant is free to twist and slide left-to-right, and front-to-back, as well as rotate.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. 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 ...The 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...Mobi-C Cervical Disc is an FDA approved artificial cervical disc for one and two level disc replacement and helps those with degenerative disc disease maintain neck mobility. Unlike fusion procedures, Mobi-C implants fits entirely within the disc space and attempts to maintain neck movement.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 ...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 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 – 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.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 ...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. The Mobi-C® Cervical Disc 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,Feb 22, 2020 · Mobi C vs Prodisc C Removal. I read an article you wrote where you commented on having successfully removed Pro-Disc C from an anterior approach without too much difficulty. Have you had the same success removing Mobi-c? Sadly I have both and the Mobi-c has been a nightmare, while the Prodisc C is holding up. The changes in clinical and radiological measures were comparable between M6-C and Mobi-C prostheses. Thirty-seven out of 52 spinal segments (71.2%) and 10 out of 16 spinal segments (62.5%) developed HO in M6-C and Mobi-C group respectively. There was no significant difference in the rate of HO between the two groups.Mobi-C Prestige ST Prodisc C 26 Lumbar ADR 22857 Total disc arthroplasty (artificial disc), anterior approach, including discectomy to prepare interspace (other than for decompression), single interspace, lumbar 0163T each additional interspace, lumbar (List separatelyAug 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 ... J Neurosurg Spine. 2014;21(4):516-28., 3 Hisey MS, Zigler JE, Jackson R, et al. Prospective, Randomized Comparison of One-level Mobi-C Cervical Total Disc Replacement vs. Anterior Cervical Discectomy and Fusion: Results at 5-year Follow-up. Int J Spine Surg. 2016;10:10. 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 FDA approved artificial cervical disc for one and two level disc replacement and helps those with degenerative disc disease maintain neck mobility. Unlike fusion procedures, Mobi-C implants fits entirely within the disc space and attempts to maintain neck movement.The 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.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.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 ...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 ... An artificial disc like Mobi-C is an option instead of a fusion that will also be placed inside the disc space to restore height and remove pressure on the pinched nerves. However, the Mobi-C device is designed to allow the neck to maintain normal motion and potentially prevent the adjacent levels from degenerating, possibly preventing future ...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 ... Jan 10, 2019 · This is a surgical video of a cervical disc replacement with the Zimmer Biomet Mobi-C TDR for treatment of a large C5-6 extruded disc herniation resulting in... An infection at the surgery site, such as a skin rash or infected cut. A known allergy to what Mobi-C is made of: cobalt, chromium, molybdenum, titanium, hydroxyapatite, polyethylene, and other trace elements. Talk to your doctor if you have a metal allergy. Damaged cervical vertebrae from an accident (trauma) at one of the surgery levels. 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 ). 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 ...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 ... 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.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 contiguous levels. This treatment is...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.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.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 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 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.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 aCervical 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.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.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 ...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. 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 ...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 ...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. Dec 1, 2022 · 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® 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 contiguous levels. This treatment is...The Healthy Neck. The neck (cervical spine) is made up of the bones (vertebrae), spinal cord, nerves, muscles, ligaments, and the system that carries blood (blood vessels). The top seven vertebrae make up the cervical spine and begin at the base of the skull. The vertebrae of the cervical spine protect the spinal cord and support the skull. 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 ...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.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 Cervical Disc is an FDA approved artificial cervical disc for one and two level disc replacement and helps those with degenerative disc disease maintain neck mobility. Unlike fusion procedures, Mobi-C implants fits entirely within the disc space and attempts to maintain neck movement. Restoring natural motion to the cervical spine. The controlled mobility of the patented mobile core is the foundation of Mobi-C. With vertebrae and neck muscle movement, the Mobi-C implant is free to twist and slide left-to-right, and front-to-back, as well as rotate. 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 titaniumDec 8, 2017 · 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 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 ... An artificial disc like Mobi-C is an option instead of a fusion that will also be placed inside the disc space to restore height and remove pressure on the pinched nerves. However, the Mobi-C device is designed to allow the neck to maintain normal motion and potentially prevent the adjacent levels from degenerating, possibly preventing future ...The changes in clinical and radiological measures were comparable between M6-C and Mobi-C prostheses. Thirty-seven out of 52 spinal segments (71.2%) and 10 out of 16 spinal segments (62.5%) developed HO in M6-C and Mobi-C group respectively. There was no significant difference in the rate of HO between the two groups.The Mobi-C® Cervical Disc Prosthesis (Mobi-C®) is a single use device for cervical intervertebral disc replacement at one level from C3 to C7 in order to maintain/restore segmental motion and disc height. The components of the Mobi-C® include a cobalt, chromium, molybdenum 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 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.Restoring natural motion to the cervical spine. The controlled mobility of the patented mobile core is the foundation of Mobi-C. With vertebrae and neck muscle movement, the Mobi-C implant is free to twist and slide left-to-right, and front-to-back, as well as rotate. The Healthy Neck. The neck (cervical spine) is made up of the bones (vertebrae), spinal cord, nerves, muscles, ligaments, and the system that carries blood (blood vessels). The top seven vertebrae make up the cervical spine and begin at the base of the skull. The vertebrae of the cervical spine protect the spinal cord and support the skull. 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 ... 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. 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 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 ...Mobi-C Cervical Disc is an FDA approved artificial cervical disc for one and two level disc replacement and helps those with degenerative disc disease maintain neck mobility. Unlike fusion procedures, Mobi-C implants fits entirely within the disc space and attempts to maintain neck movement.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. J Neurosurg Spine. 2014;21(4):516-28., 3 Hisey MS, Zigler JE, Jackson R, et al. Prospective, Randomized Comparison of One-level Mobi-C Cervical Total Disc Replacement vs. Anterior Cervical Discectomy and Fusion: Results at 5-year Follow-up. Int J Spine Surg. 2016;10:10.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. 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 ...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 ... 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.Mobi-C Prestige ST Prodisc C 26 Lumbar ADR 22857 Total disc arthroplasty (artificial disc), anterior approach, including discectomy to prepare interspace (other than for decompression), single interspace, lumbar 0163T each additional interspace, lumbar (List separatelyThe 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 ...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 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 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.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.The 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.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 ...
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. . How much is a mcdonaldpercent27s cheeseburger
J Neurosurg Spine. 2014;21(4):516-28., 3 Hisey MS, Zigler JE, Jackson R, et al. Prospective, Randomized Comparison of One-level Mobi-C Cervical Total Disc Replacement vs. Anterior Cervical Discectomy and Fusion: Results at 5-year Follow-up. Int J Spine Surg. 2016;10:10. Apr 1, 2019 · 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. 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 contiguous levels. This treatment is...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 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 Methods: This was a prospective study of patients treated with CDA at 1 or 2 contiguous levels using the Mobi-C® Cervical Disc (Zimmer Biomet). Following completion of the 7-yr Food and Drug Administration postapproval study, follow-up continued to 10 yr for consenting patients at 9 high-enrolling centers.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 ... 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.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 ). 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 ... 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.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 ...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 ...Mobi-C Prestige ST Prodisc C 26 Lumbar ADR 22857 Total disc arthroplasty (artificial disc), anterior approach, including discectomy to prepare interspace (other than for decompression), single interspace, lumbar 0163T each additional interspace, lumbar (List separatelyAn infection at the surgery site, such as a skin rash or infected cut. A known allergy to what Mobi-C is made of: cobalt, chromium, molybdenum, titanium, hydroxyapatite, polyethylene, and other trace elements. Talk to your doctor if you have a metal allergy. Damaged cervical vertebrae from an accident (trauma) at one of the surgery levels. 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. The Mobi-C Cervical Disc is one of the most widely used cervical discs in the world. First implanted in France in November 2004, Mobi-C has now been implanted in more than 75,000 spinal levels in 25 countries. Mobi-C is intended for adult patients (skeletally mature) with arm pain and/or neurological symptoms (such as weakness or numbness) with ...Cervical 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.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..
