FDA 510(k) Applications Submitted by SHAVAWN EVANS PARDUHN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K973837	10/08/1997	CLS STEM, WAGNER REVISION STEM, ALLOCLASSIC ZWEYMULLER STEM, SL	SULZER ORTHOPEDICS, INC.
K970705	02/26/1997	INTER-OP POROUS REVISION SHELL WITH SEALABLE SCREWHOLES	SULZER ORTHOPEDICS, INC.
K970706	02/26/1997	INTER-OP POROUS PROTRUSIO SHELL WITH SEALABLE SCREWHOLES	SULZER ORTHOPEDICS, INC.
K991143	04/05/1999	MAGNA-ROM 21 KNEE SYSTEEM	SULZER ORTHOPEDICS, INC.
K961589	04/24/1996	APR FULLY TEXTURED HIP STEM	INTERMEDICS ORTHOPEDICS
K961921	05/17/1996	APR OVERSIZED HIP STEM	INTERMEDICS ORTHOPEDICS
K981211	04/02/1998	APR -T REVISION HIP STEM	SULZER ORTHOPEDICS, INC.
K983509	10/07/1998	INTER-OP ACETABULAR SYSTEM - DURASUL ACETABULAR INSERT	SULZER ORTHOPEDICS, INC.