FDA 510(k) Applications Submitted by BECKY DITTY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170242	01/26/2017	MultiGenÖ 2 RF Generator System	STRYKER CORPORATION
K080450	02/19/2008	STRYKER POWER TOOL NAVIGATOR ATTACHMENT	STRYKER CORP.
K050615	03/09/2005	STRYKER NAVIGATION SYSTEM - CT-BASED HIP MODULE, MODEL 6007-621-000	STRYKER INSTRUMENTS
K141551	06/11/2014	PROFESS SOFTWARE, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 90 (DEGREES)	STRYKER CORPORATE
K162062	07/26/2016	AVAmax Vertebral Balloon, AVAflex Vertebral Balloon	STRYKER CORPORATION
K072271	08/15/2007	STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE	STRYKER CORP.
K153240	11/09/2015	Styrker OrthoMap Express Knee System	STRYKER CORPORATE
K143597	12/18/2014	Navigated XIA 4.5 Polyaxial Screwdriver	STRYKER CORPORATE
K091606	06/03/2009	VERTAPLEX HV (SINGLE PACK AND DUAL PACK)	STRYKER CORP.
K093419	11/02/2009	IVAS 2-10MM (10 GAUGE) BALLOON CATHETER, IVAS 2-15 MM(10 GAUGE)0705-115-500, IVAS 3-10MM(8 GAUGE)BALLOON CATHETER, IVAS	STRYKER INSTRUMENTS, INSTRUMENTS DIV.