The following data is part of a premarket notification filed by Zavation Medical Products Llc with the FDA for Labyrinth.
Device ID | K211306 |
510k Number | K211306 |
Device Name: | LABYRINTH |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Zavation Medical Products LLC 220 Lakeland Parkway Flowood, MS 39232 |
Contact | Colby Williams |
Correspondent | Colby Williams Zavation Medical Products LLC 220 Lakeland Parkway Flowood, MS 39232 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-04-29 |
Decision Date | 2021-06-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LABYRINTH 97762533 not registered Live/Pending |
Moog Music, Inc. 2023-01-20 |
LABYRINTH 97438634 not registered Live/Pending |
Labyrinth Games and Puzzles LLC 2022-06-01 |
LABYRINTH 90331439 not registered Live/Pending |
Miyong technology com.ltd. 2020-11-19 |
LABYRINTH 90016737 not registered Live/Pending |
Zavation Medical Products, LLC 2020-06-23 |
LABYRINTH 88585366 not registered Live/Pending |
Perfecta Federal, LLC 2019-08-20 |
LABYRINTH 88209326 not registered Live/Pending |
Labyrinth Lindon, LLC 2018-11-28 |
LABYRINTH 88143784 not registered Live/Pending |
Labyrinth Lindon, LLC 2018-10-04 |
LABYRINTH 88012397 not registered Live/Pending |
Sun, Guantong 2018-06-23 |
LABYRINTH 88012397 not registered Live/Pending |
Qin, Juying 2018-06-23 |
LABYRINTH 88012395 not registered Live/Pending |
Sun, Guantong 2018-06-23 |
LABYRINTH 88012395 not registered Live/Pending |
Qin, Juying 2018-06-23 |
LABYRINTH 88009600 not registered Live/Pending |
He, Shuhan 2018-06-21 |