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 |