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Globus Medical secure-c cervical artificial disc
Secure C Cervical Artificial Disc, supplied by Globus Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secure-c+cervical+artificial+disc/secure+c+cervical+artificial+disc/10__1097_slash_bsd__0000000000001636-105-37-41
Average 90 stars, based on 1 article reviews
secure-c cervical artificial disc - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Imaging Current Spine Hardware: Part 1, Cervical Spine and Fracture Fixation
Article Snippet: Received November 10, 2013; accepted after revision February 18, 2014. sion and low-profile hardware designs were created to reduce nonunion and hardware-related complications, respectively.. New materials are also available for use in treatment of vertebral body compression fractures.. With these new materials and designs, there are potentially new complications to detect on radiography, CT, and MRI.

Article Title: The Top 100 Cited Articles on Cervical Disc Arthroplasty
Article Snippet: Results: The results revealed a significant increase in the number of publications related to CDA over the past 2 decades, with most of the articles being published in orthopedic and spine surgery journals.. The most frequently cited articles were related to clinical outcomes, complications, and biomechanical studies of CDA.. Co-authorship analysis identified influential authors and collaborative networks, highlighting the multidisciplinary nature of CDA research involving neurosurgeons, orthopedic surgeons, and engineers.

Article Title: Clinical Outcomes With Selectively Constrained SECURE-C Cervical Disc Arthroplasty
Article Snippet: DOI: 10.1097/BRS.0000000000000031 Study Design.. Prospective, multicenter, randomized, and controlled Investigational Device Exemption clinical trial.. Objective.

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial
Article Snippet: 4 , 5 This study reports the 7-year safety and effectiveness data of the SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc, a selectively constrained cervical total disc replacement (CTDR) device.

Article Title: Solid radiographic fusion with a nonconstrained device 5 years after cervical arthroplasty
Article Snippet: Anterior cervical discectomy and fusion (ACDF) is the gold standard in the treatment of degenerative disc disease and acute disc herniation, with proven successful outcomes.. Excellent clinical and radiographic results have been seen in 85%–95% of all patients.16,17 As some studies show that fusion alters cervical spine biomechanics,4 there has been some debate whether ACDF causes adjacent-segment disease.. As a result of this concern, cervical disc arthroplasty (CDA) has emerged as a treatment option that is specifically designed to preserve segmental motion.

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial
Article Snippet: Background This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial
Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).



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Globus Medical secure-c cervical artificial disc
Secure C Cervical Artificial Disc, supplied by Globus Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secure-c+cervical+artificial+disc/secure+c+cervical+artificial+disc/10__1097_slash_bsd__0000000000001636-105-37-41
Average 90 stars, based on 1 article reviews
secure-c cervical artificial disc - by Bioz Stars, 2026-09
90/100 stars
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Globus Medical cervical artificial disc secure®-c
Cervical Artificial Disc Secure® C, supplied by Globus Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Globus Medical cervical artificial disc secure-c
Mean neck disability index (NDI) scores (+SD) for the randomized SECURE-C and anterior cervical <t>discectomy</t> and fusion (ACDF) groups through 84 months postoperative.
Cervical Artificial Disc Secure C, supplied by Globus Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secure-c+cervical+artificial+disc/secure+c+cervical+artificial+disc/pmc06159663-27-25-17
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Globus Medical secure -c cervical artificial disc
Summary of available wear testing data for cervical disc replacements under idealized (Mode I) conditions
Secure C Cervical Artificial Disc, supplied by Globus Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Mean neck disability index (NDI) scores (+SD) for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Mean neck disability index (NDI) scores (+SD) for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Mean visual analog scale (VAS) neck pain scores (+SD) for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Mean visual analog scale (VAS) neck pain scores (+SD) for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Mean visual analog scale (VAS) right arm pain scores (+SD) for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Mean visual analog scale (VAS) right arm pain scores (+SD) for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Mean 36-Item Short Form Health Survey (Mental Composite Score [MCS] and Physical Composite Score [PCS]) scores for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Mean 36-Item Short Form Health Survey (Mental Composite Score [MCS] and Physical Composite Score [PCS]) scores for the randomized SECURE-C and anterior cervical discectomy and fusion (ACDF) groups through 84 months postoperative.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Cumulative secondary surgeries at treated level by at least 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Cumulative secondary surgeries at treated level by at least 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Mean flexion-extension range of motion (ROM) at the operated level through 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Mean flexion-extension range of motion (ROM) at the operated level through 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Mean translation range of motion (ROM) at the operated level through 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Mean translation range of motion (ROM) at the operated level through 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Cumulative adjacent level surgeries through 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Journal: International Journal of Spine Surgery

Article Title: Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

doi: 10.14444/5044

Figure Lengend Snippet: Cumulative adjacent level surgeries through 84 months postoperative. Abbreviation: ACDF, anterior cervical discectomy and fusion.

Article Snippet: This research was initiated to compare the long-term clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF).

Techniques:

Summary of available wear testing data for cervical disc replacements under idealized (Mode I) conditions

Journal: Clinical Orthopaedics and Related Research

Article Title: Are PEEK-on-Ceramic Bearings an Option for Total Disc Arthroplasty? An In Vitro Tribology Study

doi: 10.1007/s11999-016-5041-7

Figure Lengend Snippet: Summary of available wear testing data for cervical disc replacements under idealized (Mode I) conditions

Article Snippet: SSED for PMA Number: P100003 (SECURE ® -C Cervical Artificial Disc) [ ] , SECURE ® -C (Globus Medical, Audubon, PA, USA) , UHMWPE on CoCr , N/A , FE: ± 7.0° LB: ± 7.0° AR: ± 1.5° (Test I) and ± 6.0° (Test II) AL: 150 N F: 2.0 Hz , As published: Test I: 2.57 ± 1.21 mg/MC Test II: 0.89 ± 0.3 mg/MC Converted (density = 0.94 mg/mm 3 ): Test I: 2.73 ± 1.29 mm 3 /MC Test I: 0.95 ± 0.32 mm 3 /MC , N/A.

Techniques: