FDA 510(k) Applications Submitted by Elias Ketchum

FDA 510(k) Number	Submission Date	Device Name	Applicant
K111410	05/19/2011	NUVASIVE LONG LATERAL SPINAL SYSTEM	NUVASIVE, INC.
K121619	06/01/2012	NUVASIVE POLYAXIAL SPINAL SCREWS	NUVASIVE, INC.
K111811	06/27/2011	BENDINI(TM) SPINAL ROD BENDING SYSTEM	NUVASIVE, INC.
K122081	07/16/2012	NUVASIVE LONG LATERAL SPINAL SYSTEM	NUVASIVE, INC.
K122352	08/03/2012	NUVASIVE PRECEPT SPINAL SYSTEM	NUVASIVE, INC.
K112709	09/19/2011	STIMULATION/DISSECTION INSTRUMENTS	NUVASIVE, INCORPORATED
K112717	09/19/2011	NUVASIVE NVJJB SYSTEM	NUVASIVE, INC.
K112718	09/19/2011	NUVASIVE NVM5 SYSTEM	NUVASIVE, INC.
K103750	12/23/2010	NUVASIVE TRAVERSE PLATE SYSTEM	NUVASIVE, INC.