FDA 510(k) Applications Submitted by ROBIN L ROWE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K150301	02/06/2015	NavSuite3 Kit	Stryker Leibinger GmbH & Co. KG - Navigation
K000594	02/22/2000	LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE	STRYKER LEIBINGER
K010969	04/02/2001	NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES	STRYKER INSTRUMENTS
K011381	05/07/2001	HUMMER IV MICRODEBRIDER SYSTEM	STRYKER INSTRUMENTS
K012380	07/26/2001	MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPY	STRYKER LEIBINGER
K032473	08/12/2003	DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE	STRYKER INSTRUMENTS
K002619	08/23/2000	NEWGEN SYSTEM	STRYKER INSTRUMENTS
K003486	11/13/2000	STEREOTACTIC FRAME BASED SYSTEM	STRYKER INSTRUMENTS
K013775	11/13/2001	TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM	STRYKER LEIBINGER
K003660	11/28/2000	LEIBINGER NEURO CLIP SYSTEM	STRYKER INSTRUMENTS
K014263	12/27/2001	NEWGEN/UNIVERSAL MANDIBULAR SYSTEM	STRYKER INSTRUMENTS