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 |