The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Vanguard 360 Revision Knee System.
| Device ID | K093293 | 
| 510k Number | K093293 | 
| Device Name: | VANGUARD 360 REVISION KNEE SYSTEM | 
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer | 
| Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 | 
| Contact | Gary Baker | 
| Correspondent | Gary Baker BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587  | 
| Product Code | JWH | 
| CFR Regulation Number | 888.3560 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2009-10-21 | 
| Decision Date | 2010-10-22 | 
| Summary: | summary |