The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Vanguard 360 Osseoti Tibial Sleeve Augment.
| Device ID | K140883 |
| 510k Number | K140883 |
| Device Name: | VANGUARD 360 OSSEOTI TIBIAL SLEEVE AUGMENT |
| Classification | Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer |
| Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
| Contact | John Heckaman |
| Correspondent | John Heckaman BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
| Product Code | MBH |
| CFR Regulation Number | 888.3565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-07 |
| Decision Date | 2014-07-30 |
| Summary: | summary |