TrellOss™-L MPF

Intervertebral Fusion Device With Bone Graft, Lumbar

Nexxt Spine LLC

The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Trelloss™-l Mpf.

Pre-market Notification Details

Device IDK192687
510k NumberK192687
Device Name:TrellOss™-L MPF
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant Nexxt Spine LLC 14425 Bergen Blvd, Suite B Noblesville,  IN  46060
ContactAndy Elsbury
CorrespondentKaren E Warden
BackRoads Consulting PO Box 566 Chesterland,  OH  44026
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2019-09-26
Decision Date2020-01-09

NIH GUDID Devices

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Trademark Results [TrellOss]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRELLOSS
TRELLOSS
88401530 not registered Live/Pending
Zimmer Biomet Spine, Inc.
2019-04-25

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