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Sintea Biotech, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K082679 LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.XJEC2009-04-07 View
510(k) K081631 SINTEA BIOTECH PLS MULTI-AXIAL SCREWSMNH2008-07-18 View
510(k) K072198 X-VOID, SPIDERHRX2008-06-06 View
510(k) K070181 SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XXMQP2007-04-18 View
510(k) K060513 SINTEA BIOTECH PLS MULTI-AXIAL SCREWS, MODEL PLS.XX.T5.XKWP2006-03-10 View
510(k) K043355 SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM WITH POLYAXIAL AND RECOVERY SCREWS, MODEL PLS.01.T5.XKWP2004-12-17 View
510(k) K041989 SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.XKWQ2004-09-16 View
510(k) K031154 SINTEA BIOTECH SCHANZ SCREW, MODEL TFX.SS.XX.XJDW2003-06-24 View
510(k) K020085 SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.XMNH2002-12-10 View
510(k) K022065 SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.XJEC2002-08-06 View
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