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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.
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