FDA 510(k) Applications Submitted by BIORETEC LTD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130716	03/15/2013	BIORETEC ACTIVASCREW INTERFERENCE	BIORETEC LTD
K080879	03/31/2008	ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM	BIORETEC LTD
K061164	04/26/2006	ACTIVAPIN	BIORETEC LTD
K081392	05/19/2008	BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN	BIORETEC LTD
K071863	07/06/2007	ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS)	BIORETEC LTD
K062980	09/29/2006	ACTIVASCREW	BIORETEC LTD
K072848	10/04/2007	ACTIVASCREW	BIORETEC LTD