The effect of implant size and device keel on vertebral compression properties in lumbar total disc replacement
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FDA device/drug status: not applicable.
Author disclosures: JDA (consulting, Synthes Spine, DePuy Spine, Paradigm Spine, LLC, research support: staff and/or materials, Synthes Spine, Fonar, Inc.; grants, DePuy Spine); RAB (consulting, Synthes; speaking and/or teaching arrangements, Synthes; trips/travel, Synthes); DME (grants, AO Spine Foundation).
PII: S1529-9430(10)00044-6
doi:10.1016/j.spinee.2010.01.008
© 2010 Elsevier Inc. All rights reserved.
