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 |