KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4

Implant, Endosseous, Root-form

SOADCO, S.L.

The following data is part of a premarket notification filed by Soadco, S.l. with the FDA for Klockner Dental Implants, Models Sk, Nk, Ik, S3, And S4.

Pre-market Notification Details

Device IDK010132
510k NumberK010132
Device Name:KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4
ClassificationImplant, Endosseous, Root-form
Applicant SOADCO, S.L. AV FITER I ROSSELL 4 BIS LOCAL 2 Escaldes-engordany,  AD Ad-700
ContactMercedes Roldan
CorrespondentMercedes Roldan
SOADCO, S.L. AV FITER I ROSSELL 4 BIS LOCAL 2 Escaldes-engordany,  AD Ad-700
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-01-16
Decision Date2002-06-04

NIH GUDID Devices

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