Sintea Biotech, Inc.
Sintea Biotech, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2009.
Top product codes for Sintea Biotech, Inc.
Recent clearances by Sintea Biotech, Inc.
- K082679 — LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X
- K081631 — SINTEA BIOTECH PLS MULTI-AXIAL SCREWS
- K072198 — X-VOID, SPIDER
- K070181 — SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XX
- K060513 — SINTEA BIOTECH PLS MULTI-AXIAL SCREWS, MODEL PLS.XX.T5.X
- K043355 — SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM WITH POLYAXIAL AND RECOVERY SCREWS, MODEL PLS.01.T5.X
- K041989 — SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X
- K031154 — SINTEA BIOTECH SCHANZ SCREW, MODEL TFX.SS.XX.X
- K020085 — SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X
- K022065 — SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X
Data sourced from openFDA. This site is unofficial and independent of the FDA.