The following data is part of a premarket notification filed by Degen Medical with the FDA for Degen Medical E3 Mis Pedicle Screw System.
| Device ID | K173814 |
| 510k Number | K173814 |
| Device Name: | DeGen Medical E3 MIS Pedicle Screw System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Degen Medical 1321-C North Cashua Drive Florence, SC 29501 |
| Contact | Craig Black |
| Correspondent | Linda Braddon, Ph.d. Secure BioMed Evaluations 7828 Hickory Flat Highway, Suite 120 Woodstock, GA 30188 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-15 |
| Decision Date | 2018-01-29 |
| Summary: | summary |