FDA 510(k) Applications Submitted by BIOCOMPOSITES LTD.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040265	02/05/2004	LITTLE GRAFTER SCREW	BIOCOMPOSITES LTD.
K040600	03/08/2004	GENEX BONE GRAFT SUBSTITUTE	BIOCOMPOSITES LTD.
K021351	04/29/2002	BIOSTEON CROSS PIN	BIOCOMPOSITES LTD.
K021551	05/13/2002	STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT	BIOCOMPOSITES LTD.
K033792	12/05/2003	BILOK ST SCREW	BIOCOMPOSITES LTD.
K003954	12/21/2000	STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT	BIOCOMPOSITES LTD.
K002070	07/07/2000	BIOLOK SCREW	BIOCOMPOSITES LTD.
K003641	11/27/2000	BIOLOK SCREW, BIOSTEON SCREW	BIOCOMPOSITES LTD.
K993238	09/27/1999	FORTOSS-CEMA	BIOCOMPOSITES LTD.
K141830	07/07/2014	STIMULAN KIT, STIMULAN RAPID CURE	BIOCOMPOSITES LTD.
K082383	08/19/2008	FORTOSS VITAL	BIOCOMPOSITES LTD.
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.
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.
K082381	08/19/2008	GENEX	BIOCOMPOSITES LTD.
K073341	11/28/2007	GENEX PUTTY	BIOCOMPOSITES LTD.
K001724	06/06/2000	STIMULAN -CALCIUM SULFATE BONE VOID FILTER	BIOCOMPOSITES LTD.
K043514	12/20/2004	ALLOGRAN-N-BONE VOID FILLER	BIOCOMPOSITES LTD.