LABYRINTH

Intervertebral Fusion Device With Bone Graft, Lumbar

Zavation Medical Products LLC

The following data is part of a premarket notification filed by Zavation Medical Products Llc with the FDA for Labyrinth.

Pre-market Notification Details

Device IDK211306
510k NumberK211306
Device Name:LABYRINTH
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant Zavation Medical Products LLC 220 Lakeland Parkway Flowood,  MS  39232
ContactColby Williams
CorrespondentColby Williams
Zavation Medical Products LLC 220 Lakeland Parkway Flowood,  MS  39232
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-04-29
Decision Date2021-06-24

Trademark Results [LABYRINTH]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LABYRINTH
LABYRINTH
90331439 not registered Live/Pending
Miyong technology com.ltd.
2020-11-19
LABYRINTH
LABYRINTH
90016737 not registered Live/Pending
Zavation Medical Products, LLC
2020-06-23
LABYRINTH
LABYRINTH
88585366 not registered Live/Pending
Perfecta Federal, LLC
2019-08-20
LABYRINTH
LABYRINTH
88209326 not registered Live/Pending
Labyrinth Lindon, LLC
2018-11-28
LABYRINTH
LABYRINTH
88143784 not registered Live/Pending
Labyrinth Lindon, LLC
2018-10-04
LABYRINTH
LABYRINTH
88012397 not registered Live/Pending
Sun, Guantong
2018-06-23
LABYRINTH
LABYRINTH
88012397 not registered Live/Pending
Qin, Juying
2018-06-23
LABYRINTH
LABYRINTH
88012395 not registered Live/Pending
Sun, Guantong
2018-06-23
LABYRINTH
LABYRINTH
88012395 not registered Live/Pending
Qin, Juying
2018-06-23
LABYRINTH
LABYRINTH
88009600 not registered Live/Pending
He, Shuhan
2018-06-21
LABYRINTH
LABYRINTH
87957365 not registered Live/Pending
Hill, Ariki, J
2018-06-11
LABYRINTH
LABYRINTH
87822556 5580338 Live/Registered
Labyrinth LLC
2018-03-06

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