S-LIF INTERVERTEBRAL BODY FUSION DEVICE

Intervertebral Fusion Device With Bone Graft, Lumbar

SPINEFRONTIER, INC.

The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for S-lif Intervertebral Body Fusion Device.

Pre-market Notification Details

Device IDK092815
510k NumberK092815
Device Name:S-LIF INTERVERTEBRAL BODY FUSION DEVICE
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly,  MA  01915
ContactJohn Sullivan
CorrespondentJohn Sullivan
SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly,  MA  01915
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeAbbreviated
3rd Party ReviewedNo
Combination ProductNo
Date Received2009-09-14
Decision Date2010-06-30
Summary:summary

NIH GUDID Devices

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