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 |