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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.
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