FDA 510(k) Applications Submitted by JOHN ROSS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K202186	08/04/2020	TrueRelief Device	TrueRelief
K190691	03/18/2019	Pixx2430 Digital Diagnostic X-Ray Receptor Panel	Pixxgen Corporation
K180976	04/13/2018	PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels	Pixxgen Corporation
K201172	05/01/2020	CFP-3131, CFP-2222	MX Imaging, Inc.
K152151	08/03/2015	ATAL 9	ATLAIM CORPORATION
K102284	08/12/2010	KRYSTALRAD 560 (FLAATZ 560)	MEDICATECH USA
K102285	08/12/2010	KRYSTALRAD (ATAL8)	MEDICATECH USA
K182533	09/14/2018	PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels	Pixxgen Corporation
K161173	04/26/2016	Avenue« T TLIF Cage	LDR SPINE USA, INC.
K163621	12/22/2016	Vitoss Bioactive (BA) Injectable	Orthovita, Inc.