FDA 510(k) Applications Submitted by MARIANNE GRUNWALDT

FDA 510(k) Number Submission Date Device Name Applicant
K020085 01/10/2002 SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X SINTEA BIOTECH, INC.
K031154 04/11/2003 SINTEA BIOTECH SCHANZ SCREW, MODEL TFX.SS.XX.X SINTEA BIOTECH, INC.
K022065 06/25/2002 SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X SINTEA BIOTECH, INC.
K070816 03/26/2007 PERIPHERAL GUIDING SHEATH MICRUS DESIGN TECHNOLOGY, INC.


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