Sintea Biotech, Inc.
10 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X (K082679) | Sintea Biotech, Inc. | 2009-04-07 |
| SINTEA BIOTECH PLS MULTI-AXIAL SCREWS (K081631) | Sintea Biotech, Inc. | 2008-07-18 |
| X-VOID, SPIDER (K072198) | Sintea Biotech, Inc. | 2008-06-06 |
| SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XX (K070181) | Sintea Biotech, Inc. | 2007-04-18 |
| SINTEA BIOTECH PLS MULTI-AXIAL SCREWS, MODEL PLS.XX.T5.X (K060513) | Sintea Biotech, Inc. | 2006-03-10 |
| SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM WITH POLYAXIAL AND RECOVERY SCREWS, MODEL PLS.01.T5.X (K043355) | Sintea Biotech, Inc. | 2004-12-17 |
| SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X (K041989) | Sintea Biotech, Inc. | 2004-09-16 |
| SINTEA BIOTECH SCHANZ SCREW, MODEL TFX.SS.XX.X (K031154) | Sintea Biotech, Inc. | 2003-06-24 |
| SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X (K020085) | Sintea Biotech, Inc. | 2002-12-10 |
| SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X (K022065) | Sintea Biotech, Inc. | 2002-08-06 |
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Every clearance here is in the API, with alerts when new ones post.