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 |