FDA 510(k) Applications Submitted by CARLOS GONZALEZ

FDA 510(k) Number Submission Date Device Name Applicant
K100112 01/14/2010 SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA, YYY=LENGTH-IN MM) SONOMA ORTHOPEDIC PRODUCTS, INC.
K090304 02/06/2009 WAVEON WRX BONE FIXATION SYSTEM SONOMA ORTHOPEDIC PRODUCTS, INC.
K081703 06/17/2008 MYGLUCOHEALTH GLUCOSE MONITORING SYSTEMS ENTRA HEALTH SYSTEMS, LTD.
K972584 07/10/1997 STRYKER HUMMER II MICRODEBRIDER SYSTEM Stryker Endoscopy
K092110 07/14/2009 WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX) SONOMA ORTHOPEDIC PRODUCTS, INC.
K113446 11/21/2011 VIGNET TELEHEALTH MANAGER VIGNET INC.


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