The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Zimmer Nexgen Complete Knee Solution Tibial And Femoral Augments.
| Device ID | K152494 |
| 510k Number | K152494 |
| Device Name: | Zimmer NexGen Complete Knee Solution Tibial And Femoral Augments |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Contact | Mark D Warner |
| Correspondent | Mark D Warner ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-01 |
| Decision Date | 2015-11-25 |
| Summary: | summary |