FDA 510(k) Applications Submitted by SARAH MARIE FITZGERALD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K121732	06/13/2012	CANOPY LAMINOPLASTY FIXATION SYSTEM	GLOBUS MEDICAL INC.
K120092	01/11/2012	PLYMOUTH THORACOLUMBAR PLATE SYSTEM	GLOBUS MEDICAL INC.
K121107	04/12/2012	FORTIFY INTEGRATED CORPECTOMY SPACERS, (FORTIFY I AND FORTIFY I-R)	GLOBUS MEDICAL, INC.
K111479	05/27/2011	REVERE CROSSTOP	GLOBUS MEDICAL INC.
K113395	11/17/2011	REVERE 4.5 STABILIZATION SYSTEM	GLOBUS MEDICAL INC.
K123783	12/10/2012	ELLIPSE OCCIPITO-CERICO-THORACIC SPINAL SYSTEM AND CAPITOL IMPLANTS	GLOBUS MEDICAL, INC.
K124058	12/31/2012	CREO STABILIZATION SYSTEM	GLOBUS MEDICAL INC.
K130392	02/15/2013	KINEX BIOACTIVE	GLOBUS MEDICAL INC.
K130478	02/25/2013	SUSTAIN AND SUSTAIN RADIOLUCENT SPACERS	GLOBUS MEDICAL, INC.
K130977	04/09/2013	SIGNIFY BIOACTIVE	GLOBUS MEDICAL INC.
K111449	05/25/2011	REVOLVE ADDITIONAL IMPLANTS	GLOBUS MEDICAL, INC.
K180079	01/10/2018	Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Activation	Hill-Rom Inc.