ASTRA TECH IMPLANT SYSTEM

Implant, Endosseous, Root-form

ASTRA TECH AB

The following data is part of a premarket notification filed by Astra Tech Ab with the FDA for Astra Tech Implant System.

Pre-market Notification Details

Device IDK101732
510k NumberK101732
Device Name:ASTRA TECH IMPLANT SYSTEM
ClassificationImplant, Endosseous, Root-form
Applicant ASTRA TECH AB 11234 EL CAMINO REAL, SUITE 200 San Diego,  CA  92130
ContactLinda K Schulz
CorrespondentLinda K Schulz
ASTRA TECH AB 11234 EL CAMINO REAL, SUITE 200 San Diego,  CA  92130
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2010-06-21
Decision Date2011-02-23
Summary:summary

Trademark Results [ASTRA TECH IMPLANT SYSTEM]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ASTRA TECH IMPLANT SYSTEM
ASTRA TECH IMPLANT SYSTEM
79029738 3280223 Live/Registered
Dentsply IH AB
2005-12-08

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