ProLift® Expandable System

Intervertebral Fusion Device With Bone Graft, Lumbar

Life Spine Inc.

The following data is part of a premarket notification filed by Life Spine Inc. with the FDA for Prolift® Expandable System.

Pre-market Notification Details

Device IDK173182
510k NumberK173182
Device Name:ProLift® Expandable System
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant Life Spine Inc. 13951 S Quality Drive Huntley,  IL  60142
ContactRandy Lewis
CorrespondentRandy Lewis
Life Spine Inc. 13951 S Quality Drive Huntley,  IL  60142
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-09-29
Decision Date2017-12-20
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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Trademark Results [ProLift]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PROLIFT
PROLIFT
88481969 not registered Live/Pending
Waterrox Investments, LLC
2019-06-20
PROLIFT
PROLIFT
87271661 not registered Live/Pending
Seville Classics Inc.
2016-12-16
PROLIFT
PROLIFT
86599032 4855635 Live/Registered
EGYED DESTINY
2015-04-15
PROLIFT
PROLIFT
86574562 5319833 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-24
PROLIFT
PROLIFT
86574549 5319832 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-24
PROLIFT
PROLIFT
86572881 5211561 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-23
PROLIFT
PROLIFT
86572878 5207129 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-23
PROLIFT
PROLIFT
86563074 4947699 Live/Registered
Rocky Mountain Vacuum Brokers LLC
2015-03-13
PROLIFT
PROLIFT
86538320 4949158 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-02-18
PROLIFT
PROLIFT
86340264 4811118 Live/Registered
Safe-T-Shade, Inc.
2014-07-17
PROLIFT
PROLIFT
86238663 4783625 Live/Registered
Beaty, Mark M.
2014-04-01
PROLIFT
PROLIFT
85435041 not registered Dead/Abandoned
Handy Button Machine Co.
2011-09-29

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