Determination of the in vivo posterior loading environment of the Coflex interlaminar-interspinous implant
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FDA device/drug status: not applicable.
Author disclosures: FTT (stock ownership, private investments, Paradigm Spine, LLC; others, ACES GmbH); GLL (stock ownership, private investments, trips/travel, other office, Paradigm Spine, LLC); JAH (stock ownership, Medical Metrics, Inc; other office, Medical Metrics, Inc; grants, DARPA); RJC (stock ownership, private investments, Paradigm Spine, LLC; others, MCRA, LLC).
PII: S1529-9430(09)01052-3
doi:10.1016/j.spinee.2009.10.010
© 2010 Elsevier Inc. All rights reserved.
