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 |