FDA 510(k) Applications Submitted by WESLEY L REED

FDA 510(k) Number Submission Date Device Name Applicant
K060095 01/13/2006 MODIFICATION TO: VACLOK SYRINGE WRIGHT MEDICAL TECHNOLOGY, INC.
K070525 02/23/2007 CHARLOTTE 7.0 MULTI-USE COMPRESSION SCREW AND WASHER WRIGHT MEDICAL TECHNOLOGY, INC.
K070592 03/02/2007 SMALL BONE WEDGE WRIGHT MEDICAL TECHNOLOGY, INC.
K060731 03/20/2006 EVOLVE MODULAR RADIAL HEAD WRIGHT MEDICAL TECHNOLOGY, INC.
K050819 03/31/2005 CHARLOTTE SNAP-OFF SCREW WRIGHT MEDICAL TECHNOLOGY, INC.
K051884 07/12/2005 CHARLOTTE SMALL MTP FUSION PLATE WRIGHT MEDICAL TECHNOLOGY, INC.
K051908 07/14/2005 CHARLOTTE COMPRESSION PLATE WRIGHT MEDICAL TECHNOLOGY, INC.
K062173 07/31/2006 MODIFICATION TO BONE GRAFT SYRINGE WRIGHT MEDICAL TECHNOLOGY, INC.
K043102 11/09/2004 MULTI-USE COMPRESSION SCREW WRIGHT MEDICAL TECHNOLOGY, INC.
K053136 11/09/2005 5TH METATARSAL FRACTURE SCREW WRIGHT MEDICAL TECHNOLOGY, INC.
K043281 11/26/2004 CHARLOTTE HIGH-DEMAND COMPRESSION SCREW WRIGHT MEDICAL TECHNOLOGY, INC.
K043583 12/28/2004 CHARLOTTE SNAP-OFF SCREW, MODELS 45110001, 45110002, 45110003 WRIGHT MEDICAL TECHNOLOGY, INC.


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