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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
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