The following data is part of a premarket notification filed by Gbs Commonwealth Co., Ltd. with the FDA for Peridot Intervertebral Body Fusion System.
| Device ID | K192026 |
| 510k Number | K192026 |
| Device Name: | Peridot Intervertebral Body Fusion System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | GBS Commonwealth Co., Ltd. C-309, Woolim Lion's Valley, 168, Gasan Digital 1-ro Geumcheon-gu, KR 08507 |
| Contact | Jimmy Kim |
| Correspondent | Jimmy Kim GBS Commonwealth Co., Ltd. C-309, Woolim Lion's Valley, 168, Gasan Digital 1-ro Geumcheon-gu, KR 08507 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-07-29 |
| Decision Date | 2019-11-26 |
| Summary: | summary |