The following data is part of a premarket notification filed by Ldr Spine Usa with the FDA for Roi-c Titanium-coated Implant System.
Device ID | K151934 |
510k Number | K151934 |
Device Name: | ROI-C Titanium-Coated Implant System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | LDR SPINE USA 13785 RESEARCH BOULEVARD, SUITE 200 Austin, TX 78750 |
Contact | James Wilson |
Correspondent | James Wilson LDR SPINE USA 13785 RESEARCH BOULEVARD, SUITE 200 Austin, TX 78750 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-07-14 |
Decision Date | 2015-12-07 |
Summary: | summary |