The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Legion Cone System.
Device ID | K162775 |
510k Number | K162775 |
Device Name: | Legion Cone System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Smith & Nephew, Inc. 7135 Goodlett Farms Parkway Cordova, TN 38016 |
Contact | Natalie Williams |
Correspondent | Dongeun Kim Smith & Nephew, Inc. 1450 Brooks Road 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 | 2016-10-03 |
Decision Date | 2017-01-13 |
Summary: | summary |