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 |