The following data is part of a premarket notification filed by Degen Medical with the FDA for Hyper-c Anterior Cervical Plate System.
Device ID | K150759 |
510k Number | K150759 |
Device Name: | Hyper-C Anterior Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Degen Medical 1321-C North Cashua Drive Florence, SC 29501 |
Contact | Craig Black |
Correspondent | Linda Braddon SECURE BIOMED EVALUATIONS 7828 HICKORY FLAT HIGHWAY Suite 120 Woodstock, GA 30188 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-23 |
Decision Date | 2015-07-28 |
Summary: | summary |