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 | K152726 |
| 510k Number | K152726 |
| Device Name: | JOURNEY II XR Knee System |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | SMITH & NEPHEW, INC. 7135 GOODLETT FARMS PARKWAY Cordova, TN 38016 |
| Contact | Brad Sheals |
| Correspondent | Brad Sheals SMITH & NEPHEW, INC. 7135 GOODLETT FARMS PARKWAY Cordova, TN 38016 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-22 |
| Decision Date | 2015-10-21 |
| Summary: | summary |