FDA 510(k) Applications Submitted by Simon Fitzer

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050170	01/26/2005	FORTOSS VITAL BONE GRAFT SUBSTITUTE	BIOCOMPOSITES LTD.
K071091	04/18/2007	MODIFICATION TO BILOK SCREW	BIOCOMPOSITES LTD.
K071115	04/20/2007	MODIFICATION TO BILOK ST SCREW	BIOCOMPOSITES LTD.
K061311	05/10/2006	ALLOGRAN-R	BIOCOMPOSITES LTD.
K991662	05/14/1999	TITANIUM HARTSHILL SYSTEM	SURGICRAFT LTD.
K081428	05/21/2008	MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR	BIOCOMPOSITES LTD.
K061949	07/10/2006	DOUBLEPLAY SUTURE ANCHOR	BIOCOMPOSITES LTD.
K071952	07/16/2007	GRAFTLOCK SCREW, ST SCREW	BIOCOMPOSITES LTD.
K072127	08/02/2007	DOMINATOR	BIOCOMPOSITES LTD.
K982719	08/04/1998	THE BONE TIE	SURGICRAFT LTD.
K082381	08/19/2008	GENEX	BIOCOMPOSITES LTD.
K212721	08/27/2021	Genex Bone Graft Substitute	Biocomposites Ltd
K073341	11/28/2007	GENEX PUTTY	BIOCOMPOSITES LTD.