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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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