JULIET LL LATERAL LUMBAR CAGE

Intervertebral Fusion Device With Bone Graft, Lumbar

SPINEART

The following data is part of a premarket notification filed by Spineart with the FDA for Juliet Ll Lateral Lumbar Cage.

Pre-market Notification Details

Device IDK133557
510k NumberK133557
Device Name:JULIET LL LATERAL LUMBAR CAGE
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant SPINEART COINTRIN 20 ROUTE DE PRE-BOIS CP1813 Geneva,  CH 1215
ContactFranck Pennesi
CorrespondentFranck Pennesi
SPINEART COINTRIN 20 ROUTE DE PRE-BOIS CP1813 Geneva,  CH 1215
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-11-19
Decision Date2014-02-03
Summary:summary

NIH GUDID Devices

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