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 |