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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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