FDA 510(k) Applications Submitted by STRYKER LEIBINGER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K022579	08/05/2002	STRYKER NAVIGATION SYSTEM-KNEE MODULE	STRYKER LEIBINGER
K023449	10/15/2002	NON-INVASIVE PATIENT FIXATION SYSTEM	STRYKER LEIBINGER
K000348	02/03/2000	COLORADO MICRODISSECTION NEEDLE	STRYKER LEIBINGER
K000349	02/03/2000	MOTORIZED MICRO MULTILEAF COLLIMATOR	STRYKER LEIBINGER
K991398	04/22/1999	BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KIT	STRYKER LEIBINGER
K000594	02/22/2000	LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE	STRYKER LEIBINGER
K012380	07/26/2001	MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPY	STRYKER LEIBINGER
K013775	11/13/2001	TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM	STRYKER LEIBINGER
K040022	01/07/2004	STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM	STRYKER LEIBINGER
K041651	06/17/2004	STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM	STRYKER LEIBINGER
K052871	10/11/2005	STRYKER CUSTOM TI IMPLANT	STRYKER LEIBINGER
K043250	11/23/2004	STRYKER PATIENT SPECIFIC POLYMER IMPLANT	STRYKER LEIBINGER