The following data is part of a premarket notification filed by Solco Biomedical Co., Ltd. with the FDA for 4cis® Marlin Acif Cage System.
| Device ID | K162402 |
| 510k Number | K162402 |
| Device Name: | 4CIS® Marlin ACIF Cage System |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | SOLCO BIOMEDICAL CO., LTD. 154 SEOTAN-RO, SEOTAN-MYEON Pyeongtaek, KR 17704 |
| Contact | Kim Il |
| Correspondent | Hwi Joon Park FIRST GOLD CORP. 14110 DALLAS PKWY, SUITE 135 Dallas, TX 75254 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-08-26 |
| Decision Date | 2017-02-16 |
| Summary: | summary |