The following data is part of a premarket notification filed by Spinal Elements Inc. with the FDA for Lucent®.
Device ID | K170235 |
510k Number | K170235 |
Device Name: | Lucent® |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Spinal Elements Inc. 3115 Melrose Dr., Suite 200 Carlsbad, CA 92010 |
Contact | Julie Lamothe |
Correspondent | Julie Lamothe Spinal Elements Inc. 3115 Melrose Dr., Suite 200 Carlsbad, CA 92010 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-01-25 |
Decision Date | 2017-11-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LUCENT 98363852 not registered Live/Pending |
Applied Materials, Inc. 2024-01-18 |
![]() LUCENT 98362973 not registered Live/Pending |
Habby, LLC 2024-01-18 |
![]() LUCENT 98351345 not registered Live/Pending |
Dayah, Michael J. 2024-01-10 |
![]() LUCENT 98302177 not registered Live/Pending |
Kotzeva, Mariana 2023-12-06 |
![]() LUCENT 97531251 not registered Live/Pending |
Ocaso Group LLC 2022-08-02 |
![]() LUCENT 97359144 not registered Live/Pending |
Schneller LLC 2022-04-12 |
![]() LUCENT 97118936 not registered Live/Pending |
Smart, LLC 2021-11-10 |
![]() LUCENT 90977139 not registered Live/Pending |
Lucent Surgical Support Systems, Inc. 2021-05-11 |
![]() LUCENT 90865531 not registered Live/Pending |
Lucent Industry Co., Ltd. 2021-08-04 |
![]() LUCENT 90703416 not registered Live/Pending |
Lucent Surgical Support Systems, Inc. 2021-05-11 |
![]() LUCENT 90459149 not registered Live/Pending |
Swarovski Aktiengesellschaft 2021-01-11 |
![]() LUCENT 87679949 not registered Dead/Abandoned |
Modne, Inc. 2017-11-10 |