PAO Cortical Screw

Screw, Fixation, Bone

Medacta International SA

The following data is part of a premarket notification filed by Medacta International Sa with the FDA for Pao Cortical Screw.

Pre-market Notification Details

Device IDK211435
510k NumberK211435
Device Name:PAO Cortical Screw
ClassificationScrew, Fixation, Bone
Applicant Medacta International SA Strada Regina Castel San Pietro,  CH Ch-6874
ContactStefano Baj
CorrespondentChris Lussier
Medacta USA 3973 Delp Street Memphis,  TN  83118
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-05-10
Decision Date2021-08-06

NIH GUDID Devices

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