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 |