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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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