DISCOVERY

Intervertebral Fusion Device With Bone Graft, Cervical

INTUITIVE SPINE, LLC

The following data is part of a premarket notification filed by Intuitive Spine, Llc with the FDA for Discovery.

Pre-market Notification Details

Device IDK111484
510k NumberK111484
Device Name:DISCOVERY
ClassificationIntervertebral Fusion Device With Bone Graft, Cervical
Applicant INTUITIVE SPINE, LLC 33490 PIN OAK PARKWAY Avon Lake,  OH  44012
ContactJennifer Palinchik
CorrespondentJennifer Palinchik
INTUITIVE SPINE, LLC 33490 PIN OAK PARKWAY Avon Lake,  OH  44012
Product CodeODP  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2011-05-31
Decision Date2011-09-12
Summary:summary

NIH GUDID Devices

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