BIO-VENT IMPLANT

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 Bio-vent Implant.

Pre-market Notification Details

Device IDK950575
510k NumberK950575
Device Name:BIO-VENT IMPLANT
ClassificationImplant, Endosseous, Root-form
Applicant CORE-VENT CORP. 4630 SOUTH ARVILLE STE D Las Vegas,  NV  89103
ContactGlen Neally
CorrespondentGlen Neally
CORE-VENT CORP. 4630 SOUTH ARVILLE STE D Las Vegas,  NV  89103
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-01-27
Decision Date1995-07-11

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