The following data is part of a premarket notification filed by Depuy (ireland) with the FDA for Attune Revision Knee System.
Device ID | K160700 |
510k Number | K160700 |
Device Name: | ATTUNE Revision Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Depuy (Ireland) Loughbeg Ringaskiddy Co. Cork Munster, IE |
Contact | Jaime Weeks |
Correspondent | Soraya L. Hori DePuy Orthopaedics, Inc. 700 Orthopaedic Drive Warsaw, IN 46582 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-14 |
Decision Date | 2016-06-10 |
Summary: | summary |