FDA 510(k) Applications Submitted by INTERNAL FIXATION SYSTEMS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K110086 01/12/2011 IFS PROFILE PLATES, SCREWS, AND WASHERS INTERNAL FIXATION SYSTEMS, INC.
K113399 11/17/2011 IFS SUBTALAR IMPLANT INTERNAL FIXATION SYSTEMS, INC.
K071035 04/12/2007 IFS BONE FIXATION DEVICES INTERNAL FIXATION SYSTEMS, INC.
K061620 06/09/2006 IFS CANNULATED BONE SCREW INTERNAL FIXATION SYSTEMS, INC.


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