The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Journey Ii Xr Knee System.
Device ID | K141471 |
510k Number | K141471 |
Device Name: | JOURNEY II XR KNEE SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | SMITH & NEPHEW, INC. 7135 GOODLET FARM PARKWAY Cordova, TN 38018 |
Contact | Shereen Bienz |
Correspondent | Shereen Bienz SMITH & NEPHEW, INC. 7135 GOODLET FARM PARKWAY Cordova, TN 38018 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-06-03 |
Decision Date | 2014-11-14 |
Summary: | summary |