EVERSTICK POST

Post, Root Canal

STICK TECH LTD.

The following data is part of a premarket notification filed by Stick Tech Ltd. with the FDA for Everstick Post.

Pre-market Notification Details

Device IDK030820
510k NumberK030820
Device Name:EVERSTICK POST
ClassificationPost, Root Canal
Applicant STICK TECH LTD. 80 PARKWAY WEST Mount Vernon,  NY  10552
ContactWilliam Troetel
CorrespondentWilliam Troetel
STICK TECH LTD. 80 PARKWAY WEST Mount Vernon,  NY  10552
Product CodeELR  
CFR Regulation Number872.3810 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-03-14
Decision Date2003-05-20
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
J0229008271 K030820 000
15400556008673 K030820 000
15400556008666 K030820 000
15400556008659 K030820 000

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