FDA 510(k) Applications Submitted by Gerd Federle

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170890	03/27/2017	TELIX K Interbody System	Biedermann Motech GmbH & Co. KG
K181821	07/09/2018	MOSS VRS Spinal System	Biedermann Motech GmbH & Co. KG
K162232	08/08/2016	MOSS 100 Pedicle Screw System	Biedermann Motech GmbH & Co. KG
K203607	12/10/2020	MOSS VRS Spinal System	Biedermann Motech GmbH & Co. KG