Life Spine ALIF Buttress Plate System

Appliance, Fixation, Spinal Intervertebral Body

Life Spine, Inc.

The following data is part of a premarket notification filed by Life Spine, Inc. with the FDA for Life Spine Alif Buttress Plate System.

Pre-market Notification Details

Device IDK222628
510k NumberK222628
Device Name:Life Spine ALIF Buttress Plate System
ClassificationAppliance, Fixation, Spinal Intervertebral Body
Applicant Life Spine, Inc. 13951 S. Quality Drive Huntley,  IL  60142
ContactAngela Batker
CorrespondentAngela Batker
Life Spine, Inc. 13951 S. Quality Drive Huntley,  IL  60142
Product CodeKWQ  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2022-08-31
Decision Date2022-11-16

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