FDA 510(k) Applications Submitted by ROBERT SHERIDAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K022233	07/10/2002	HYDROBOOT	INCAPPE, INC.
K073643	12/26/2007	TRANS1 AXIALIF 2-LEVEL OR II SYSTEM	TRANS1 INCORPORATED
K970233	01/21/1997	GELBFISH ENDO-VAC SYSTEM	GARY A. GELBFISH
K961027	03/14/1996	ORTHOFIX TIBIAL NAILING SYSTEM	ORTHOFIX, INC.
K050965	04/18/2005	TRANS1 AXIALIF SYSTEM	TRANS1 INCORPORATED
K961725	05/03/1996	OSCAR ORTHOSONICS SYSTEM FOR CEMENTED ARTHROPLASTY REVISION	C.L. MCINTOSH & ASSOC., INC.
K991580	05/07/1999	ILM ENDOTRACHEAL TUBE	THE LARYNGEAL MASK CO.,LTD.
K051856	07/08/2005	TRANS1 FACET SCREWS	TRANS1 INCORPORATED
K962699	07/11/1996	RADWORKS MEDICAL IMAGING SOFTWARE	APPLICARE MEDICAL IMAGING, B.V.
K973944	10/16/1997	ORTHOFIX FEMORAL NAILING SYTEM	ORTHOFIX SRL
K003446	11/06/2000	SYMMETRY AORTIC CLIP SYSTEM	ST. JUDE MEDICAL CARDIOVASCULAR GROUP, INC.
K974186	11/07/1997	ORTHOFIX EXTERNAL FIXATION SCREW (PIN) WITH HYDROXYAPATITE COATING	ORTHOFIX SRL
K955848	12/27/1995	ORTHOFIX MODULSYSTEM	ORTHOFIX, INC.