The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Cetra Anterior Cervical Plate System.
Device ID | K162638 |
510k Number | K162638 |
Device Name: | CETRA Anterior Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Contact | Jacki Koch |
Correspondent | Jacki Koch Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-09-22 |
Decision Date | 2016-12-16 |
Summary: | summary |