FDA 510(k) Applications Submitted by Benjamin A Kimball

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120177	01/20/2012	SPINAL ELEMENTS CERCLAGE SYSTEM	SPINAL ELEMENTS, INC.
K120467	02/15/2012	SPINAL ELEMENTS POSTERIOR CERVICAL/THORACIC SPINAL SYSTEM	SPINAL ELEMENTS, INC.
K110632	03/04/2011	LUCENT OR LUCENT MAGNUM	SPINAL ELEMENTS, INC.
K150588	03/09/2015	OVA1 Next Generation	VERMILLION, INC.
K131427	05/17/2013	LOTUS	SPINAL ELEMENTS, INC.
K101848	07/01/2010	SAPPHIRE ANTERIOR CERVICAL PLATE SYSTEM	SPINAL ELEMENTS, INC.
K122771	09/10/2012	SPINAL ELEMENTS CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM	SPINAL ELEMENTS, INC.
K122967	09/25/2012	LUCENT	SPINAL ELEMENTS, INC.