ALAMO C

Intervertebral Fusion Device With Bone Graft, Cervical

ALLIANCE PARTNERS, LLC

The following data is part of a premarket notification filed by Alliance Partners, Llc with the FDA for Alamo C.

Pre-market Notification Details

Device IDK133321
510k NumberK133321
Device Name:ALAMO C
ClassificationIntervertebral Fusion Device With Bone Graft, Cervical
Applicant ALLIANCE PARTNERS, LLC 33490 PIN OAK PARKWAY Avon Lake,  OH  44012
ContactJennifer Palinchik
CorrespondentJennifer Palinchik
ALLIANCE PARTNERS, LLC 33490 PIN OAK PARKWAY Avon Lake,  OH  44012
Product CodeODP  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-10-29
Decision Date2014-01-09
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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