FDA 510(k) Applications Submitted by SARAH FAIRFIELD

FDA 510(k) Number Submission Date Device Name Applicant
K120593 02/28/2012 MYOSURE CONTROL UNIT HOLOGIC, INC.
K120947 03/29/2012 THS INSTRUMENT TRAY HOLOGIC, INC.
K101074 04/19/2010 MODIFICATION TO: CD HORIZON(R) SPINAL SYSTEM MEDTRONIC SOFAMOR DANEK USA, INC.
K131581 05/31/2013 MYOSURE TISSUE REMOVAL DEVICE (1 PACK AND 3 PACK) HOLOGIC, INC.
K131736 06/13/2013 MYOSURE TISSUE REMOVAL DEVICE (1 PACK), MYOSURE TISSUE REMOVAL DEVICE (3 PACK) HOLOGIC, INC.
K121868 06/26/2012 MYOSURE LITE TISSUE REMOVAL DEVICE (1 PACK), MYOSURE LITE TISSUE REMOVAL DEVICE (3 PACK) HOLOGIC, INC.
K092201 07/22/2009 ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE WRIGHT MEDICAL TECHNOLOGY, INC.
K142029 07/25/2014 MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM HOLOGIC, INC.
K122498 08/16/2012 MYOSURE XL TISSUE REMOVAL DEVICE (1 PACK) MYOSURE XL TISSUE REMOVAL DEVICE (3 PACK) HOLOGIC, INC.
K122563 08/22/2012 MYOSURE XL ROD LENS HYSTEROSCOPE, MYOSURE XL OUTLFOW CHANNEL HOLOGIC, INC.
K163052 11/01/2016 Brevera Biopsy System with Corlumina Imaging Technology HOLOGIC, INC.
K153486 12/04/2015 Affirm Prone Biopsy System Hologic Inc


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