The following data is part of a premarket notification filed by Smith & Nephew Inc with the FDA for Journey Ii Unicompartmental Knee System.
| Device ID | K190085 |
| 510k Number | K190085 |
| Device Name: | Journey II Unicompartmental Knee System |
| Classification | Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer |
| Applicant | Smith & Nephew Inc 7135 Goodlett Farms Parkway Cordova, TN 38016 |
| Contact | Amy Winegarden |
| Correspondent | Amy Winegarden Smith & Nephew Inc 7135 Goodlett Farms Parkway Cordova, TN 38016 |
| Product Code | HSX |
| Subsequent Product Code | KRR |
| Subsequent Product Code | NPJ |
| CFR Regulation Number | 888.3520 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-01-17 |
| Decision Date | 2019-02-11 |
| Summary: | summary |