FDA 510(k) Applications Submitted by JEAN SHEPPARD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K072118	08/01/2007	STRYKER VERTAPLEX RADIOPAQUE BONE CEMENT	STRYKER CORP.
K063480	11/17/2006	STRYKER RF INTRADISCAL ADAPTOR, MODEL 406-750	STRYKER CORP.
K043442	12/14/2004	STRYKER RF COAXIAL BIPOLAR ELECTRODES & CANNULAE	STRYKER INSTRUMENTS
K040300	02/09/2004	STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE)	STRYKER INSTRUMENTS
K040369	02/13/2004	STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM	STRYKER INSTRUMENTS
K050753	03/23/2005	STRYKER DISCMONITOR	STRYKER INSTRUMENTS
K061835	06/29/2006	STRYKER SILVERGLIDE BIPOLAR FORCEPS REUSABLE CABLE; DISPOSABLE CABLE	STRYKER INSTRUMENTS
K032117	07/09/2003	STRYKER TOTAL PERFORMANCE (TPS) SYSTEM	STRYKER INSTRUMENTS
K032303	07/25/2003	STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM	STRYKER INSTRUMENTS