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.
Device ID | K210961 |
510k Number | K210961 |
Device Name: | U2 Total Knee System, XPE Tibial Insert, PS PLUS |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | United Orthopedic Corporation No 57, Park Ave 2, Science Park Hsinchu, TW 30075 |
Contact | Lois Ho |
Correspondent | Lois Ho United Orthopedic Corporation No 57, Park Ave 2, Science Park Hsinchu, TW 30075 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-03-31 |
Decision Date | 2021-04-21 |
Summary: | summary |