FDA 510(k) Applications Submitted by SINTEA BIOTECH, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K081631 |
06/11/2008 |
SINTEA BIOTECH PLS MULTI-AXIAL SCREWS |
SINTEA BIOTECH, INC. |
| K082679 |
09/15/2008 |
LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X |
SINTEA BIOTECH, INC. |
| K043355 |
12/06/2004 |
SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM WITH POLYAXIAL AND RECOVERY SCREWS, MODEL PLS.01.T5.X |
SINTEA BIOTECH, INC. |
| K070181 |
01/19/2007 |
SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XX |
SINTEA BIOTECH, INC. |
| K060513 |
02/27/2006 |
SINTEA BIOTECH PLS MULTI-AXIAL SCREWS, MODEL PLS.XX.T5.X |
SINTEA BIOTECH, INC. |
| K072198 |
08/07/2007 |
X-VOID, SPIDER |
SINTEA BIOTECH, INC. |
| K041989 |
07/23/2004 |
SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X |
SINTEA BIOTECH, INC. |
| 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. |
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