The following data is part of a premarket notification filed by Nvision Biomedical Technologies, Llc with the FDA for Healix™ Compression Screw System.
Device ID | K182949 |
510k Number | K182949 |
Device Name: | Healix™ Compression Screw System |
Classification | Screw, Fixation, Bone |
Applicant | Nvision Biomedical Technologies, LLC 4754 Shavano Oak, Suite 101 San Antonio, TX 78249 |
Contact | Diana Langham |
Correspondent | Jeffrey Brittan Watershed Idea Foundry 1815 Aston Ave., Suite 106 Carlsbad, CA 92008 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-10-23 |
Decision Date | 2018-12-04 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HEALIX 98073918 not registered Live/Pending |
Healix Clinical Laboratory LLC 2023-07-06 |
HEALIX 97113462 not registered Live/Pending |
Sciessent LLC 2021-11-08 |
HEALIX 88731594 not registered Live/Pending |
Ubican Global Licensing, LLC 2019-12-18 |
HEALIX 87931155 not registered Dead/Abandoned |
NVision Biomedical Technologies, LLC 2018-05-22 |
HEALIX 87080602 not registered Dead/Abandoned |
Medtronic, Inc. 2016-06-22 |
HEALIX 85938034 not registered Dead/Abandoned |
Advanced Suture, Inc. 2013-05-21 |
HEALIX 85932954 not registered Dead/Abandoned |
Haber, Jeff 2013-05-15 |
HEALIX 85852688 4435372 Live/Registered |
HEALIX INFUSION THERAPY, LLC 2013-02-18 |
HEALIX 85822252 not registered Dead/Abandoned |
Healix International Limited 2013-01-14 |
HEALIX 78232622 3101469 Live/Registered |
HEALIX INFUSION THERAPY, LLC 2003-04-01 |
HEALIX 78231329 3098782 Live/Registered |
HEALIX INFUSION THERAPY, LLC 2003-03-28 |
HEALIX 78231318 3098781 Live/Registered |
HEALIX INFUSION THERAPY, LLC 2003-03-28 |