FDA 510(k) Applications Submitted by WADE T RUTKOSKIE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040022	01/07/2004	STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM	STRYKER LEIBINGER
K060061	01/09/2006	STRYKER INJECTABLE CEMENT	STRYKER CORP.
K030378	02/05/2003	STRYKER LEIBINGER CRANIAL FIXATION SYSTEM	STRYKER INSTRUMENTS
K060750	03/21/2006	STRYKER INJECTABLE CEMENT	STRYKER CMF
K060763	03/21/2006	STRYKER INJECTABLE CEMENT	Stryker
K021440	05/06/2002	BONESOURCE HAC	STRYKER INSTRUMENTS
K031659	05/28/2003	UNIVERSAL NEURO SYSTEM	STRYKER INSTRUMENTS
K051603	06/15/2005	STRYKER INJECTABLE CEMENT	STRYKER LEIBINGER MICRO IMPLANTS
K041651	06/17/2004	STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM	STRYKER LEIBINGER
K022185	07/03/2002	UNIVERSAL CMF SYSTEM	STRYKER INSTRUMENTS
K032366	08/01/2003	BONESOURCE HAC FAST SETTING CEMENT	STRYKER INSTRUMENTS
K033232	10/06/2003	COLORADO MICRODISSECTION NEEDLE	STRYKER CORP.
K052871	10/11/2005	STRYKER CUSTOM TI IMPLANT	STRYKER LEIBINGER
K043250	11/23/2004	STRYKER PATIENT SPECIFIC POLYMER IMPLANT	STRYKER LEIBINGER
K043334	12/03/2004	BONE SOURCE HAC RAPID SETTING CEMENT	STRYKER INSTRUMENTS