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 |