FDA 510(k) Applications Submitted by JEFFRY B SKIBA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K081977	07/11/2008	PROSIT WOUND TREATMENT DEVICE	SILVERLEAF MEDICAL PRODUCTS, INC.
K962779	07/17/1996	COMPRESSION SCREW	ORTHOPAEDIC BIOSYSTEMS, LTD.
K982963	08/24/1998	POLYMER THREADED ANCHOR / SUTURE COMBINATION	ORTHOPAEDIC BIOSYSTEMS, LTD.
K982996	08/27/1998	POLYMER OBL SB ANCHOR / SUTURE COMBINATION	ORTHOPAEDIC BIOSYSTEMS, LTD.
K963420	08/30/1996	CANCELLOUS SCREW WASHER	ORTHOPAEDIC BIOSYSTEMS, LTD.
K963432	08/30/1996	GUIDE WIRES FOR CANNULATED SCREWS	ORTHOPAEDIC BIOSYSTEMS, LTD.
K963433	08/30/1996	THREADED FIXATION PIN	ORTHOPAEDIC BIOSYSTEMS, LTD.
K983169	09/10/1998	POLYMER THREADED ANCHOR	ORTHOPAEDIC BIOSYSTEMS, LTD.