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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