The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Vanguard Ssk 360 Revision Knee System.
| Device ID | K121149 |
| 510k Number | K121149 |
| Device Name: | VANGUARD SSK 360 REVISION KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46581 -0587 |
| Contact | Gary Baker, M.s. Rac |
| Correspondent | Gary Baker, M.s. Rac BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46581 -0587 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-04-16 |
| Decision Date | 2012-05-16 |
| Summary: | summary |