FDA 510(k) Applications Submitted by Jamie Wilson

FDA 510(k) Number	Submission Date	Device Name	Applicant
K200613	03/09/2020	Tritanium« X TL Expandable Curved Posterior Lumbar Cage	Stryker Corporation
K161798	06/30/2016	FacetBRIDGE« System	LDR SPINE USA, INC.
K162133	08/01/2016	VerteFIT Corpectomy Cage System	LDR SPINE USA, INC.