FDA 510(k) Applications Submitted by MICHAEL BOTTLANG,

FDA 510(k) Number	Submission Date	Device Name	Applicant
K160633	03/07/2016	G3(TM) Active Plate(R) Small Fragment System	GENESIS FRACTURE CARE, INC.
K171293	05/02/2017	G3Ö Active Plate« Miniature System	Genesis Fracture Care, Inc.
K152242	08/10/2015	G3┐ Active Plate« Large Fragment System	GENESIS FRACTURE CARE, INC.
K142938	10/09/2014	G3 Active Plate Large Fragment System	GENESIS FRACTURE CARE, INC.
K150649	03/12/2015	G3 Active Plate Large Fragment System	GENESIS FRACTURE CARE, INC.