Sintea Biotech, Inc.
FDA 510(k) medical device clearances.
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.