VERICORE IMPLANT ABUTMENTS

Abutment, Implant, Dental, Endosseous

WHIP-MIX CORP.

The following data is part of a premarket notification filed by Whip-mix Corp. with the FDA for Vericore Implant Abutments.

Pre-market Notification Details

Device IDK082299
510k NumberK082299
Device Name:VERICORE IMPLANT ABUTMENTS
ClassificationAbutment, Implant, Dental, Endosseous
Applicant WHIP-MIX CORP. 361 FARMINGTON AVE. Louisville,  KY  40217
ContactDavid J Steinbock
CorrespondentDavid J Steinbock
WHIP-MIX CORP. 361 FARMINGTON AVE. Louisville,  KY  40217
Product CodeNHA  
CFR Regulation Number872.3630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2008-08-12
Decision Date2008-11-20
Summary:summary

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