The following data is part of a premarket notification filed by Dio Medical Co., Ltd. with the FDA for Rex Anterior Cervical Plate System.
Device ID | K121862 |
510k Number | K121862 |
Device Name: | REX ANTERIOR CERVICAL PLATE SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | DIO MEDICAL CO., LTD. 325 N. PUENTE ST UNIT B Brea, CA 92821 |
Contact | April Lee |
Correspondent | April Lee DIO MEDICAL CO., LTD. 325 N. PUENTE ST UNIT B Brea, CA 92821 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-06-26 |
Decision Date | 2012-10-31 |
Summary: | summary |