FDA 510(k) Applications Submitted by J. STEPHEN BRATT

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.