The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Journey Ii Deep Dished Articular Inserts.
Device ID | K113482 |
510k Number | K113482 |
Device Name: | JOURNEY II DEEP DISHED ARTICULAR INSERTS |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Contact | Shereen Myers |
Correspondent | Shereen Myers SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-11-23 |
Decision Date | 2012-02-27 |
Summary: | summary |