The following data is part of a premarket notification filed by Gs Medical Co., Ltd. with the FDA for Mvp Cervical Plate System.
Device ID | K190170 |
510k Number | K190170 |
Device Name: | MVP Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | GS Medical Co., Ltd. 90, Osongsaengmyeong 4-Ro Osong-eup, KR 363-951 |
Contact | Barry Sands |
Correspondent | Manjusha Bharadwaj RQMIS 110 Haverhill Road Amesbury, MA 01913 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-02-01 |
Decision Date | 2019-05-13 |
Summary: | summary |