CORE-VENT ARMENTARIUM

Implant, Endosseous, Root-form

CORE-VENT CORP.

The following data is part of a premarket notification filed by Core-vent Corp. with the FDA for Core-vent Armentarium.

Pre-market Notification Details

Device IDK900177
510k NumberK900177
Device Name:CORE-VENT ARMENTARIUM
ClassificationImplant, Endosseous, Root-form
Applicant CORE-VENT CORP. 15821 VENTURA BLVD. Encino,  CA  91436
ContactPatrick, Dds
CorrespondentPatrick, Dds
CORE-VENT CORP. 15821 VENTURA BLVD. Encino,  CA  91436
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-01-16
Decision Date1990-06-28

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