FDA 510(k) Applications Submitted by OsteoMed

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140978	04/16/2014	OSTEOMED LOW PROFILE ORBITAL FLOOR PLATE SYSTEM	OSTEOMED
K203479	11/27/2020	ExtremiLOCK Lateral Ankle Fusion Plates	OsteoMed
K140283	02/04/2014	OSTEOMED EXTREMIFUSE SYSTEM	OSTEOMED
K133437	11/07/2013	1ST MTP PLATE	OSTEOMED
K161041	04/13/2016	OsteoMed ExtremiLOCK Wrist Plating System	OSTEOMED
K162542	09/12/2016	OsteoMed PINNACLE Driver	OSTEOMED
K162544	09/12/2016	OsteoMed PINNACLE Driver	OSTEOMED
K130412	02/19/2013	OSTEOMED EXTREMIFUSE SYSTEM	OSTEOMED
K121304	05/01/2012	OSTEOMED CRANIAL DISTRACTION SYSTEM	OSTEOMED
K151195	05/04/2015	OsteoMed IMF Screw	OSTEOMED
K152145	08/03/2015	OsteoMed ExtremiLOCK Wrist Plating System	OSTEOMED
K131851	06/21/2013	OSTEOMED NEURO RONGEUR	OSTEOMED