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 |