The following data is part of a premarket notification filed by Sintea Biotech, Inc. with the FDA for Sintea Biotech Anterior Plate System, Model Acp.xx.t5.x.
| Device ID | K041989 | 
| 510k Number | K041989 | 
| Device Name: | SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X | 
| Classification | Appliance, Fixation, Spinal Intervertebral Body | 
| Applicant | SINTEA BIOTECH, INC. 407 LINCOLN RD. SUITE 10L Miami Beach, FL 33139 | 
| Contact | Isabella Elias | 
| Correspondent | Isabella Elias SINTEA BIOTECH, INC. 407 LINCOLN RD. SUITE 10L Miami Beach, FL 33139 | 
| Product Code | KWQ | 
| CFR Regulation Number | 888.3060 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2004-07-23 | 
| Decision Date | 2004-09-16 | 
| Summary: | summary |