LINK® MEGASYSTEM-C®

Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer

Waldemar Link GmbH & Co. KG

The following data is part of a premarket notification filed by Waldemar Link Gmbh & Co. Kg with the FDA for Link® Megasystem-c®.

Pre-market Notification Details

Device IDK151008
510k NumberK151008
Device Name:LINK® MEGASYSTEM-C®
ClassificationProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer
Applicant Waldemar Link GmbH & Co. KG Barkhausenweg 10 Hamburg,  DE 22339
ContactHelmut D Link
CorrespondentStefanie Reimers
Waldemar Link GmbH & Co. KG Barkhausenweg 10 Hamburg,  DE 22339
Product CodeKRO  
Subsequent Product CodeJDI
Subsequent Product CodeLWJ
Subsequent Product CodeLZO
CFR Regulation Number888.3510 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2015-04-15
Decision Date2015-08-26
Summary:summary

NIH GUDID Devices

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