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 |