METOXIT CAM-BLANKS

Powder, Porcelain

Metoxit AG

The following data is part of a premarket notification filed by Metoxit Ag with the FDA for Metoxit Cam-blanks.

Pre-market Notification Details

Device IDK072569
510k NumberK072569
Device Name:METOXIT CAM-BLANKS
ClassificationPowder, Porcelain
Applicant Metoxit AG 1705 S. CAPITAL OF TEXAS HWY SUITE 500 Austin,  TX  78746
ContactIan Gordon
CorrespondentIan Gordon
Metoxit AG 1705 S. CAPITAL OF TEXAS HWY SUITE 500 Austin,  TX  78746
Product CodeEIH  
CFR Regulation Number872.6660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-09-12
Decision Date2007-10-31
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
EMET4097900 K072569 000

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