The following data is part of a premarket notification filed by Neurostructures, Inc. with the FDA for Arco™-sa Lumbar Cage System.
Device ID | K173082 |
510k Number | K173082 |
Device Name: | Arco™-SA Lumbar Cage System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | NeuroStructures, Inc. 16 Technology Drive Suite 165 Irvine, CA 92618 |
Contact | Kathleen Wong |
Correspondent | Meredith L. May Empirical Testing Corp. 4628 Northpark Drive Colorado Springs, CO 80918 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-29 |
Decision Date | 2018-03-29 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARCO 98641129 not registered Live/Pending |
SHENZHEN IVPS TECHNOLOGY CO.,LTD. 2024-07-10 |
ARCO 98226194 not registered Live/Pending |
Unibrands Corporation 2023-10-16 |
ARCO 98120215 not registered Live/Pending |
Shed Innovations Inc. 2023-08-07 |
ARCO 97262774 not registered Live/Pending |
Modernica, Inc. 2022-02-11 |
ARCO 90570980 not registered Live/Pending |
Muraflex Inc. 2021-03-10 |
ARCO 90374623 not registered Live/Pending |
Modernica, Inc. 2020-12-11 |
ARCO 88907314 not registered Live/Pending |
Arco Marine, Inc. 2020-05-08 |
ARCO 88907291 not registered Live/Pending |
Arco Marine, Inc. 2020-05-08 |
ARCO 88627578 not registered Live/Pending |
Arco Marine Inc 2019-09-23 |
ARCO 86897569 5157652 Live/Registered |
Omicron electronics GmbH 2016-02-04 |
ARCO 86727034 5440855 Live/Registered |
LG ELECTRONICS INC. 2015-08-17 |
ARCO 86571357 4974522 Live/Registered |
Gradus Group LLC 2015-03-20 |