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FDA 510(k) Applications Submitted by INSTRATEK, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080280
02/04/2008
SUB-TALAR LOK, MODEL 7-11 MM
INSTRATEK, INC.
K120493
02/17/2012
MINI CANNULATED HEADED AND HEADLESS SCREW SET
INSTRATEK, INC.
K111032
04/13/2011
CMC CABLE FIX
INSTRATEK, INC.
K131620
06/03/2013
JONES-FX FRACTURE SYSTEM
INSTRATEK, INC.
K091763
06/16/2009
MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000
INSTRATEK, INC.
K082384
08/19/2008
HAV-LOK BUNION CORRECTION SYSTEM
INSTRATEK, INC.
K133523
11/15/2013
STAPIX SUPERELASTIC IMPLANT BONE STAPLES
INSTRATEK, INC.
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