FDA 510(k) Applications Submitted by Nvision Biomedical Technologies, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K240250 |
01/30/2024 |
3D Printed PEEK Interbody System |
Nvision Biomedical Technologies, Inc. |
| K210424 |
02/11/2021 |
Quantum Anterior Cervical Plate |
Nvision Biomedical Technologies, Inc. |
| K190380 |
02/19/2019 |
nvc |
Nvision Biomedical Technologies, Inc. |
| K230853 |
03/28/2023 |
EARP Nerve Cuff Electrode |
Nvision Biomedical Technologies, Inc. |
| K212477 |
08/09/2021 |
EARP Interbody System |
Nvision Biomedical Technologies, Inc. |
| K192645 |
09/24/2019 |
TrigonÖ Ti Stand-Alone Wedge Fixation System |
Nvision Biomedical Technologies, Inc. |
| K223226 |
10/18/2022 |
TrigonÖ HA Stand-Alone Wedge Fixation System |
Nvision Biomedical Technologies, Inc. |
| K203445 |
11/23/2020 |
Trigon HA Stand-Alone Wedge Fixation System |
Nvision Biomedical Technologies, Inc. |
| K193645 |
12/30/2019 |
nva, nvp, and nvt |
Nvision Biomedical Technologies, Inc. |
|
|
