FDA 510(k) Applications Submitted by Blesson Abraham

FDA 510(k) Number	Submission Date	Device Name	Applicant
K210016	01/04/2021	Integra DigiFuse Cannulated Intramedullary Fusion System,Integra Total Foot System,Integra CAPTURE Screw System & Integra Ti6 Internal Fixation System,Subtalar MBA System,MetaSurg Subtalar Implant,NewDeal BOLD Screw,NewDeal HALLU Lock Plate System,NewDeal	Integra Lifesciences Corporation
K140283	02/04/2014	OSTEOMED EXTREMIFUSE SYSTEM	OSTEOMED
K190588	03/07/2019	Integra TITAN Reverse Shoulder System	Integra LifeSciences Corporation
K151021	04/16/2015	OsteoMed Cannulated Screw System	OSTEOMED CORP.
K131445	05/20/2013	OSTEOMED EXTREMILOCK FOOT PLATING SYSTEM	OSTEOMED LP
K181639	06/21/2018	Panta 2 Arthrodesis Nail System	Integra Lifesciences Corporation
K181999	07/26/2018	Integra TITAN Reverse Shoulder System	Integra Lifesciences Corporation
K133437	11/07/2013	1ST MTP PLATE	OSTEOMED
K133691	12/02/2013	EXTRIMILOCK ANKLE PLATING SYSTEM	OSTEOMED LP