FDA 510(k) Applications Submitted by Nvision Biomedical Technologies, LLC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K142328 |
08/20/2014 |
nvc |
NVISION BIOMEDICAL TECHNOLOGIES, LLC |
| K142594 |
09/15/2014 |
nva, nvp, nvt |
NVISION BIOMEDICAL TECHNOLOGIES, LLC |
| K180458 |
02/20/2018 |
FOCUS Pedicle Screw System |
Nvision Biomedical Technologies, LLC |
| K182943 |
10/23/2018 |
VERTEX Nitinol Staple System |
Nvision Biomedical Technologies, LLC |
| K182949 |
10/23/2018 |
HealixÖ Compression Screw System |
Nvision Biomedical Technologies, LLC |
| K183055 |
11/02/2018 |
Vector Hammertoe Correction System |
Nvision Biomedical Technologies, LLC |
| K170074 |
01/09/2017 |
nvc |
Nvision Biomedical Technologies, LLC |
| K161524 |
06/02/2016 |
Tangis Anterior Cervical Plate |
NVISION BIOMEDICAL TECHNOLOGIES, LLC |
| K162426 |
08/30/2016 |
nva, nvp, and nvt |
NVISION BIOMEDICAL TECHNOLOGIES, LLC |
| K173091 |
09/29/2017 |
Boundary Anterior Lumbar Buttress Plate |
Nvision Biomedical Technologies, LLC |
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