U2 Total Knee System, XPE Tibial Insert, PS PLUS

Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer

United Orthopedic Corporation

The following data is part of a premarket notification filed by United Orthopedic Corporation with the FDA for U2 Total Knee System, Xpe Tibial Insert, Ps Plus.

Pre-market Notification Details

Device IDK210961
510k NumberK210961
Device Name:U2 Total Knee System, XPE Tibial Insert, PS PLUS
ClassificationProsthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
Applicant United Orthopedic Corporation No 57, Park Ave 2, Science Park Hsinchu,  TW 30075
ContactLois Ho
CorrespondentLois Ho
United Orthopedic Corporation No 57, Park Ave 2, Science Park Hsinchu,  TW 30075
Product CodeJWH  
CFR Regulation Number888.3560 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-03-31
Decision Date2021-04-21
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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