The following data is part of a premarket notification filed by Aesculap Implant Systems with the FDA for Vega Knee System.
| Device ID | K121879 |
| 510k Number | K121879 |
| Device Name: | VEGA KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | AESCULAP IMPLANT SYSTEMS 3773 CORPORATE PWKY. Center Valley, PA 18034 |
| Contact | Julie Tom Wing |
| Correspondent | Julie Tom Wing AESCULAP IMPLANT SYSTEMS 3773 CORPORATE PWKY. Center Valley, PA 18034 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-28 |
| Decision Date | 2012-07-27 |
| Summary: | summary |