FDA 510(k) Applications Submitted by CINDY DOMECUS

FDA 510(k) Number Submission Date Device Name Applicant
DEN150007 02/10/2015 Magnetic Surgical System Levita Magnetics International Corp.
K120665 03/05/2012 INVENT SNORING DEVICE VENTUS MEDICAL, INC.
K080983 04/07/2008 PROVENT NASAL CANNULA VENTUS MEDICAL, INC.
K121195 04/19/2012 NVISION VLE IMAGING SYSTEM NVISION VLE CATHETER NINEPOINT MEDICAL, INC
K061210 05/01/2006 FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01B KYPHON, INC.
K131405 05/15/2013 IFUSE IMPLANT SYSTEM SI-BONE, INC.
K071560 06/07/2007 PROVENT NASAL DILATOR, MODEL BR2 VENTUS MEDICAL, INC.
K972210 06/11/1997 RESECTOSCOPE SAFETY SHEATH CONCEPTUS, INC.
K041584 06/14/2004 KYPHX HV-R BONE CEMENT, MODEL C01A KYPHON, INC.
DEN140020 06/24/2014 ECLIPSE SYSTEM PELVALON
K122074 07/16/2012 IFUSE IMPLANT SYSTEM SI-BONE, INC.
DEN120015 08/24/2012 EEVA 2.0 AUXOGYN, INC.
K092729 09/04/2009 BAXANO NEURO CHECK DEVICE BAXANO, INC.
K954164 09/05/1995 HYSTEROSCOPE CONCEPTUS, INC.
K112770 09/23/2011 NVISION VLE IMAGING SYSTEM, NVISION VLE CATHETER NINEPOINT MEDICAL, INC
K063071 10/06/2006 DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B KYPHON, INC.
K133144 10/17/2013 SONOSURE SONOHYSTEROGRAPHY & ENDOMETRIAL SAMPLING DEVICE CrossBay Medical, Inc.
K123329 10/26/2012 DA VINVI SURGICAL SYSTEM INTUITIVE SURGICAL, INC.
K033801 12/08/2003 KYPHX HV-R, MODEL C01A KYPHON, INC.
K123850 12/14/2012 IFUSE IMPLANT SYSTEM SI-BONE, INC.
K124031 12/28/2012 DA VINCI FLUORESCENCE IMAGING VISION SYSTEM INTUITIVE SURGICAL, INC.
K141141 05/02/2014 KIVA VCF TREATMENT SYSTEM BENVENUE MEDICAL, INC.
K142023 07/25/2014 LUNA INTERBODY SYSTEM BENVENUE MEDICAL, INC.
K132817 09/09/2013 KIVA VCF TREATMENT SYSTEM BENVENUE MEDICAL, INC.
K123642 11/26/2012 MUSCLE STIMULATION SYSTEM NIVEUS MEDICAL, INC.
K120800 03/16/2012 NVISION VLE IMAGING SYSTEM NINEPOINT MEDICAL, INC.


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